{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,4]],"date-time":"2026-04-04T11:48:20Z","timestamp":1775303300043,"version":"3.50.1"},"reference-count":49,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2003,3,1]],"date-time":"2003-03-01T00:00:00Z","timestamp":1046476800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2003,3,1]],"date-time":"2003-03-01T00:00:00Z","timestamp":1046476800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Genes Immun"],"published-print":{"date-parts":[[2003,3,1]]},"DOI":"10.1038\/sj.gene.6363943","type":"journal-article","created":{"date-parts":[[2003,3,4]],"date-time":"2003-03-04T16:25:57Z","timestamp":1046795157000},"page":"138-146","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":26,"title":["Linkage disequilibrium between the MBP tetranucleotide repeat and multiple sclerosis is restricted to a geographically defined subpopulation in Finland"],"prefix":"10.1038","volume":"4","author":[{"given":"H","family":"Pihlaja","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T","family":"Rantam\u00e4ki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Wikstr\u00f6m","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M-L","family":"Sumelahti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Laaksonen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Ilonen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Ruutiainen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T","family":"Pirttil\u00e4","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I","family":"Elovaara","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Reunanen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S","family":"Kuokkanen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L","family":"Peltonen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K","family":"Koivisto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P J","family":"Tienari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2003,3,4]]},"reference":[{"key":"BF6363943_CR1","doi-asserted-by":"publisher","first-page":"1221","DOI":"10.1016\/S0140-6736(02)08220-X","volume":"359","author":"A Compston","year":"2002","unstructured":"Compston A, Coles A . Multiple sclerosis. Lancet 2002; 359: 1221\u20131231.","journal-title":"Lancet"},{"key":"BF6363943_CR2","doi-asserted-by":"publisher","first-page":"49","DOI":"10.1016\/S0165-5728(99)00081-8","volume":"98","author":"BD Trapp","year":"1999","unstructured":"Trapp BD, Bo L, Mork S, Chang A . Pathogenesis of tissue injury in MS lesions. J Neuroimmunol 1999; 98: 49\u201356.","journal-title":"J Neuroimmunol"},{"key":"BF6363943_CR3","doi-asserted-by":"publisher","first-page":"99","DOI":"10.1093\/oxfordjournals.epirev.a017951","volume":"19","author":"AD Sadovnick","year":"1997","unstructured":"Sadovnick AD, Dyment D, Ebers GC . Genetic epidemiology of multiple sclerosis. Epidemiol Rev 1997; 19: 99\u2013106.","journal-title":"Epidemiol Rev"},{"key":"BF6363943_CR4","doi-asserted-by":"publisher","first-page":"259","DOI":"10.1007\/s11910-002-0085-3","volume":"2","author":"A Compston","year":"2002","unstructured":"Compston A, Sawcer S . Genetic analysis of multiple sclerosis. Curr Neurol Neurosci Rep 2002; 2: 259\u2013266.","journal-title":"Curr Neurol Neurosci Rep"},{"key":"BF6363943_CR5","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1111\/j.1399-0039.1991.tb02029.x","volume":"38","author":"O Olerup","year":"1991","unstructured":"Olerup O, Hillert J . HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation. Tissue Antigens 1991; 38: 1\u201315.","journal-title":"Tissue Antigens"},{"key":"BF6363943_CR6","doi-asserted-by":"publisher","first-page":"1869","DOI":"10.1093\/brain\/121.10.1869","volume":"121","author":"J Chataway","year":"1998","unstructured":"Chataway J, Feakes R, Coraddu F et al. The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen. Brain 1998; 121: 1869\u20131887.","journal-title":"Brain"},{"key":"BF6363943_CR7","doi-asserted-by":"publisher","first-page":"472","DOI":"10.1038\/ng0896-472","volume":"13","author":"GC Ebers","year":"1996","unstructured":"Ebers GC, Kukay K, Bulman DE et al. A full genome search in multiple sclerosis. Nat Genet 1996; 13: 472\u2013476.","journal-title":"Nat Genet"},{"key":"BF6363943_CR8","doi-asserted-by":"publisher","first-page":"469","DOI":"10.1038\/ng0896-469","volume":"13","author":"JL Haines","year":"1996","unstructured":"Haines JL, Ter-Minassian M, Bazyk A et al. A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. Nat Genet 1996; 13: 469\u2013471.","journal-title":"Nat Genet"},{"key":"BF6363943_CR9","doi-asserted-by":"publisher","first-page":"1379","DOI":"10.1086\/301637","volume":"61","author":"S Kuokkanen","year":"1997","unstructured":"Kuokkanen S, Gschwend M, Rioux JD et al. Genomewide scan of multiple sclerosis in Finnish multiplex families. Am J Hum Genet 1997; 61: 1379\u20131387.","journal-title":"Am J Hum Genet"},{"key":"BF6363943_CR10","doi-asserted-by":"publisher","first-page":"477","DOI":"10.1038\/ng0896-477","volume":"13","author":"S Kuokkanen","year":"1996","unstructured":"Kuokkanen S, Sundvall M, Terwilliger JD et al. A putative vulnerability locus to multiple sclerosis maps to 5p14\u2013p12 in a region syntenic to the murine locus Eae2. Nat Genet 1996; 13: 477\u2013480.","journal-title":"Nat Genet"},{"key":"BF6363943_CR11","doi-asserted-by":"publisher","first-page":"456","DOI":"10.1038\/sj.gene.6363705","volume":"1","author":"F Larsen","year":"2000","unstructured":"Larsen F, Oturai A, Ryder LP et al. Linkage analysis of a candidate region in Scandinavian sib pairs with multiple sclerosis reveals linkage to chromosome 17q. Genes Immun 2000; 1: 456\u2013459.","journal-title":"Genes Immun"},{"key":"BF6363943_CR12","doi-asserted-by":"crossref","unstructured":"The Transatlantic Multiple Sclerosis Genetics Cooperative. A meta-analysis of genomic screens in multiple sclerosis. Mult Scler 2001; 7: 3\u201311.","DOI":"10.1191\/135245801669625359"},{"key":"BF6363943_CR13","doi-asserted-by":"publisher","first-page":"134","DOI":"10.1016\/S0165-5728(02)00051-6","volume":"126","author":"K Reunanen","year":"2002","unstructured":"Reunanen K, Finnil\u00e4 S, Laaksonen M et al. Chromosome 19q13 and multiple sclerosis susceptibility in Finland: linkage and two-stage association study. J Neuroimmunol 2002; 126: 134\u2013142.","journal-title":"J Neuroimmunol"},{"key":"BF6363943_CR14","doi-asserted-by":"publisher","first-page":"203","DOI":"10.1177\/135245859800400322","volume":"4","author":"P Stinissen","year":"1998","unstructured":"Stinissen P, Medaer R, Raus J . Myelin reactive T cells in the autoimmune pathogenesis of multiple sclerosis. Multiple Scleroris 1998; 4: 203\u2013211.","journal-title":"Multiple Scleroris"},{"key":"BF6363943_CR15","doi-asserted-by":"publisher","first-page":"74","DOI":"10.1111\/j.1750-3639.2001.tb00383.x","volume":"11","author":"AT Campagnoni","year":"2001","unstructured":"Campagnoni AT, Skoff RP . The pathobiology of myelin mutants reveal novel biological functions of the MBP and PLP genes. Brain Pathol 2001; 11: 74\u201391.","journal-title":"Brain Pathol"},{"key":"BF6363943_CR16","doi-asserted-by":"publisher","first-page":"291","DOI":"10.1002\/ana.410270311","volume":"27","author":"KB Boylan","year":"1990","unstructured":"Boylan KB, Takahashi N, Paty DW et al. DNA length polymorphism 5\u2032 to the myelin basic protein gene is associated with multiple sclerosis. Ann Neurol 1990; 27: 291\u2013297.","journal-title":"Ann Neurol"},{"key":"BF6363943_CR17","doi-asserted-by":"publisher","first-page":"987","DOI":"10.1016\/0140-6736(92)93007-A","volume":"340","author":"PJ Tienari","year":"1992","unstructured":"Tienari PJ, Wikstrom J, Sajantila A, Palo J, Peltonen L . Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene. Lancet 1992; 340: 987\u2013991.","journal-title":"Lancet"},{"key":"BF6363943_CR18","doi-asserted-by":"publisher","first-page":"1179","DOI":"10.1016\/0140-6736(93)91003-5","volume":"341","author":"J Rose","year":"1993","unstructured":"Rose J, Gerken S, Lynch S et al. Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene. Lancet 1993; 341: 1179\u20131181.","journal-title":"Lancet"},{"key":"BF6363943_CR19","doi-asserted-by":"publisher","first-page":"615","DOI":"10.1007\/BF00920626","volume":"241","author":"M Eoli","year":"1994","unstructured":"Eoli M, Pandolfo M, Milanese C, Gasparini P, Salmaggi A, Zeviani M . The myelin basic protein gene is not a major susceptibility locus for multiple sclerosis in Italian patients. J Neurol 1994; 241: 615\u2013619.","journal-title":"J Neurol"},{"key":"BF6363943_CR20","doi-asserted-by":"publisher","first-page":"1191","DOI":"10.1136\/jnnp.57.10.1191","volume":"57","author":"NW Wood","year":"1994","unstructured":"Wood NW, Holmans P, Clayton D, Robertson N, Compston DA . No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs. J Neurol Neurosurg Psychiatry 1994; 57: 1191\u20131194.","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"BF6363943_CR21","doi-asserted-by":"publisher","first-page":"155","DOI":"10.1007\/s100480050076","volume":"2","author":"E Seboun","year":"1999","unstructured":"Seboun E, Oksenberg JR, Rombos A et al. Linkage analysis of candidate myelin genes in familial multiple sclerosis. Neurogenetics 1999; 2: 155\u2013162.","journal-title":"Neurogenetics"},{"key":"BF6363943_CR22","doi-asserted-by":"publisher","first-page":"1596","DOI":"10.1016\/0140-6736(93)90734-X","volume":"341","author":"CA Graham","year":"1993","unstructured":"Graham CA, Kirk CW, Nevin NC et al. Lack of association between myelin basic protein gene microsatellite and multiple sclerosis. Lancet 1993; 341: 1596 (letter).","journal-title":"Lancet"},{"key":"BF6363943_CR23","doi-asserted-by":"publisher","first-page":"97","DOI":"10.1016\/0165-5728(94)90167-8","volume":"52","author":"C Vandevyver","year":"1994","unstructured":"Vandevyver C, Stinissen P, Cassiman JJ, Raus J . Myelin basic protein gene polymorphism is not associated with chronic progressive multiple sclerosis. J Neuroimmunol 1994; 52: 97\u201399.","journal-title":"J Neuroimmunol"},{"key":"BF6363943_CR24","doi-asserted-by":"publisher","first-page":"1256","DOI":"10.1001\/jama.1997.03550150060036","volume":"278","author":"LF Barcellos","year":"1997","unstructured":"Barcellos LF, Thomson G, Carrington M et al. Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients. JAMA 1997; 278: 1256\u20131261.","journal-title":"JAMA"},{"key":"BF6363943_CR25","doi-asserted-by":"publisher","first-page":"457","DOI":"10.1111\/j.1365-2990.1997.tb01322.x","volume":"23","author":"SE Price","year":"1997","unstructured":"Price SE, Sharpe G, Boots A et al. Role of myelin basic protein and proteolipid protein genes in multiple sclerosis: single strand conformation polymorphism analysis of the human sequences. Neuropathol Appl Neurobiol 1997; 23: 457\u2013467.","journal-title":"Neuropathol Appl Neurobiol"},{"key":"BF6363943_CR26","doi-asserted-by":"publisher","first-page":"46","DOI":"10.1111\/j.1600-0404.1998.tb00608.x","volume":"97","author":"B He","year":"1998","unstructured":"He B, Yang B, Lundahl J, Fredrikson S, Hillert J . The myelin basic protein gene in multiple sclerosis: identification of discrete alleles of a 1.3\u2009kb tetranucleotide repeat sequence. Acta Neurol Scand 1998; 97: 46\u201351.","journal-title":"Acta Neurol Scand"},{"key":"BF6363943_CR27","doi-asserted-by":"publisher","first-page":"158","DOI":"10.1016\/S0165-5728(97)00171-9","volume":"81","author":"PJ Tienari","year":"1998","unstructured":"Tienari PJ, Kuokkanen S, Pastinen T et al. Golli-MBP gene in multiple sclerosis susceptibility. J Neuroimmunol 1998; 81: 158\u2013167.","journal-title":"J Neuroimmunol"},{"key":"BF6363943_CR28","doi-asserted-by":"publisher","first-page":"236","DOI":"10.1111\/j.1600-0404.1996.tb00513.x","volume":"93","author":"SN Ibsen","year":"1996","unstructured":"Ibsen SN, Clausen J . A repetitive DNA sequence 5\u2032 to the human myelin basic protein gene may be linked to MS in Danes. Acta Neurol Scand 1996; 93: 236\u2013240.","journal-title":"Acta Neurol Scand"},{"issue":"Suppl 2","key":"BF6363943_CR29","first-page":"28","volume":"6","author":"FR Guerini","year":"2000","unstructured":"Guerini FR, Losciale L, Mediati M et al. A polymorphism in the repetitive (TGGA)n sequence 5\u2032 to the human myelin basic protein gene in Italian multiple sclerosis patients. J Neurovirol 2000; 6 (Suppl 2): 28\u201332.","journal-title":"J Neurovirol"},{"key":"BF6363943_CR30","doi-asserted-by":"publisher","first-page":"16","DOI":"10.1016\/0888-7543(90)90443-X","volume":"6","author":"KB Boylan","year":"1990","unstructured":"Boylan KB, Ayres TM, Popko B, Takahashi N, Hood LE, Prusiner SB . Repetitive DNA (TGGA)n 5\u2032 to the human myelin basic protein gene: a new form of oligonucleotide repetitive sequence showing length polymorphism. Genomics 1990; 6:16\u201322.","journal-title":"Genomics"},{"key":"BF6363943_CR31","doi-asserted-by":"publisher","first-page":"313","DOI":"10.1007\/BF02432126","volume":"108","author":"L Gusm\u00e3o","year":"1996","unstructured":"Gusm\u00e3o L, Amorim A, Prata MJ, Pereira L, Lareu MV, Carracedo A . Failed PCR amplifications of MBP-STR alleles due to polymorphism in the primer annealing region. Int J Legal Med 1996; 108: 313\u2013315.","journal-title":"Int J Legal Med"},{"key":"BF6363943_CR32","doi-asserted-by":"publisher","first-page":"551","DOI":"10.1016\/S0168-9525(00)02139-9","volume":"16","author":"H Ellegren","year":"2000","unstructured":"Ellegren H . Microsatellite mutations in the germline: implications for evolutionary inference. Trends Genet 2000; 16: 551\u2013558.","journal-title":"Trends Genet"},{"key":"BF6363943_CR33","doi-asserted-by":"publisher","first-page":"67","DOI":"10.1159\/000026241","volume":"19","author":"ML Sumelahti","year":"2000","unstructured":"Sumelahti ML, Tienari PJ, Wikstr\u00f6m J, Palo J, Hakama M . Regional and temporal variation in multiple sclerosis incidence in Finland during 1979\u201393. Neuroepidemiology 2000; 19: 67\u201375.","journal-title":"Neuroepidemiology"},{"key":"BF6363943_CR34","doi-asserted-by":"publisher","first-page":"153","DOI":"10.1034\/j.1600-0404.2001.103003153.x","volume":"103","author":"ML Sumelahti","year":"2001","unstructured":"Sumelahti ML, Tienari PJ, Palo Jorma, Wikstr\u00f6m J, Hakama M . Increasing prevalence of multiple sclerosis in Finland. Acta Neurol Scand 2001; 103: 153\u2013158.","journal-title":"Acta Neurol Scand"},{"key":"BF6363943_CR35","doi-asserted-by":"publisher","first-page":"478","DOI":"10.1038\/sj.gene.6363698","volume":"1","author":"H Coppin","year":"2000","unstructured":"Coppin H, Ribouchon MT, Bausero P et al. No evidence for transmission disequilibrium between a new marker at the myelin basic protein locus and multiple sclerosis in French patients. Genes Immun 2000; 1: 478\u2013482.","journal-title":"Genes Immun"},{"key":"BF6363943_CR36","doi-asserted-by":"publisher","first-page":"182","DOI":"10.1038\/35042049","volume":"1","author":"L Peltonen","year":"2000","unstructured":"Peltonen L, Palotie A, Lange K . Use of population isolates for mapping complex traits. Nat Rev Genet 2000; 1: 182\u2013190.","journal-title":"Nat Rev Genet"},{"key":"BF6363943_CR37","doi-asserted-by":"publisher","first-page":"85","DOI":"10.1111\/j.1600-0404.1975.tb01362.x","volume":"51","author":"J Wikstr\u00f6m","year":"1975","unstructured":"Wikstr\u00f6m J, Palo J . Studies on the clustering of multiple sclerosis in Finland II: comparison between the domiciles and places of birth in selected subpopulations. Acta Neurol Scand 1975; 51: 85\u201398.","journal-title":"Acta Neurol Scand"},{"key":"BF6363943_CR38","doi-asserted-by":"publisher","first-page":"173","DOI":"10.1111\/j.1600-0404.1975.tb07598.x","volume":"51","author":"J Wikstr\u00f6m","year":"1975","unstructured":"Wikstr\u00f6m J, Palo J . Studies on the clustering of multiple sclerosis in Finland II: Microepidemiology in one high-risk county with special reference to familial cases. Acta Neurol Scand 1975; 51: 173\u2013183.","journal-title":"Acta Neurol Scand"},{"key":"BF6363943_CR39","doi-asserted-by":"publisher","first-page":"74","DOI":"10.1159\/000110844","volume":"3","author":"J Wikstr\u00f6m","year":"1984","unstructured":"Wikstr\u00f6m J, Kinnunen E, Porras J . The age-specific prevalence ratio of familial multiple sclerosis. Neuroepidemiology 1984; 3: 74\u201382.","journal-title":"Neuroepidemiology"},{"key":"BF6363943_CR40","unstructured":"Sumelahti ML, Tienari PJ, Hakama M, Wikstr\u00f6m J . MS in Finland: incidence trends and differences in relapsing remitting and primary progressive disease courses. J Neurol Neurosurg Psychiatry (in press)."},{"key":"BF6363943_CR41","doi-asserted-by":"publisher","first-page":"140","DOI":"10.1016\/S0165-5728(01)00456-8","volume":"122","author":"M Laaksonen","year":"2002","unstructured":"Laaksonen M, Pastinen T, Sj\u00f6roos M et al. HLA class II associated risk and protection against multiple sclerosis\u2014a Finnish family study. J Neuroimmunol 2002; 122: 140\u2013145.","journal-title":"J Neuroimmunol"},{"key":"BF6363943_CR42","doi-asserted-by":"publisher","first-page":"257","DOI":"10.1159\/000472423","volume":"1","author":"PJ Tienari","year":"1993","unstructured":"Tienari PJ, Wikstr\u00f6m J, Koskimies S, Partanen J, Palo J, Peltonen L . Reappraisal of HLA in multiple sclerosis: close linkage in multiplex families. Eur J Hum Genet 1993; 1: 257\u2013268.","journal-title":"Eur J Hum Genet"},{"key":"BF6363943_CR43","doi-asserted-by":"publisher","first-page":"183","DOI":"10.1007\/BF01371334","volume":"106","author":"A M\u00f6ller","year":"1994","unstructured":"M\u00f6ller A, Wiegand P, Gr\u00fcschow C, Seuchter SA, Baur MP, Brinkmann B . Population data and forensic efficiency values for the STR systems HumVWA, HumMBP and HumFABP. Int J Legal Med 1994; 106: 183\u2013189.","journal-title":"Int J Legal Med"},{"key":"BF6363943_CR44","doi-asserted-by":"publisher","first-page":"138","DOI":"10.1159\/000022794","volume":"48","author":"JD Terwilliger","year":"1998","unstructured":"Terwilliger JD, Zollner S, Laan M, Paabo S . Mapping genes through the use of linkage disequilibrium generated by genetic drift: \u2018drift mapping\u2019 in small populations with no demographic expansion. Hum Hered 1998; 48: 138\u2013154.","journal-title":"Hum Hered"},{"key":"BF6363943_CR45","doi-asserted-by":"publisher","first-page":"673","DOI":"10.1086\/339258","volume":"70","author":"H Kaessmann","year":"2002","unstructured":"Kaessmann H, Zollner S, Gustafsson AC et al. Extensive linkage disequilibrium in small human populations in Eurasia. Am J Hum Gen 2002; 70: 673\u2013685.","journal-title":"Am J Hum Gen"},{"key":"BF6363943_CR46","first-page":"1","volume-title":"The History of Southern Ostrobothnia","author":"A Luukko","year":"1950","unstructured":"Luukko A . The historical settlement of Southern Ostrobothnia. In: The Southern Ostrobothnian History-Committee (ed). The History of Southern Ostrobothnia. Maalaiskuntien Liiton Kirjapaino: Helsinki, 1950, pp 1\u201381 (in Finnish)."},{"key":"BF6363943_CR47","first-page":"3","volume-title":"McAlpine's Multiple Sclerosis","author":"A Compston","year":"1999","unstructured":"Compston A . The story of multiple sclerosis. In: Compstron A, Ebers G, Lassmann H, McDonald, Matthews B, Wekerle H (eds). McAlpine's Multiple Sclerosis. Churchill-Livingstone: New York, 1999, pp 3\u201342."},{"key":"BF6363943_CR48","doi-asserted-by":"publisher","first-page":"103","DOI":"10.1111\/j.1744-313X.1993.tb00099.x","volume":"20","author":"P Westman","year":"1993","unstructured":"Westman P, Kuismin T, Partanen J, Koskimies S . An HLA-DR typing protocol using group-specific PCR-amplification followed by restriction enzyme digests. Eur J Immunogenet 1993; 20: 103\u2013109.","journal-title":"Eur J Immunogenet"},{"key":"BF6363943_CR49","doi-asserted-by":"publisher","first-page":"1170","DOI":"10.1086\/302577","volume":"65","author":"D Clayton","year":"1999","unstructured":"Clayton D . A generalization of the transmission\/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 1999; 65: 1170\u20131177.","journal-title":"Am J Hum Genet"}],"container-title":["Genes &amp; Immunity"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.nature.com\/articles\/6363943.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/6363943","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/6363943.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,3,22]],"date-time":"2022-03-22T19:13:40Z","timestamp":1647976420000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/6363943"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2003,3,1]]},"references-count":49,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2003,3,1]]}},"alternative-id":["BF6363943"],"URL":"https:\/\/doi.org\/10.1038\/sj.gene.6363943","relation":{},"ISSN":["1466-4879","1476-5470"],"issn-type":[{"value":"1466-4879","type":"print"},{"value":"1476-5470","type":"electronic"}],"subject":[],"published":{"date-parts":[[2003,3,1]]},"assertion":[{"value":"7 August 2002","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"6 September 2002","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"6 September 2002","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"4 March 2003","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}]}}