{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T03:34:07Z","timestamp":1790739247600,"version":"4.1.0"},"reference-count":24,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1996,5,1]],"date-time":"1996-05-01T00:00:00Z","timestamp":830908800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Nat Genet"],"published-print":{"date-parts":[[1996,5]]},"DOI":"10.1038\/ng0596-101","type":"journal-article","created":{"date-parts":[[2004,8,18]],"date-time":"2004-08-18T20:12:15Z","timestamp":1092859935000},"page":"101-104","source":"Crossref","is-referenced-by-count":99,"title":["The gene for hereditary sensory neuropathy type I (HSN\u2013I) maps to chromosome 9q22.1\u2013q22.3"],"prefix":"10.1038","volume":"13","author":[{"given":"Garth A.","family":"Nicholson","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer L.","family":"Dawkins","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ian P.","family":"Blair","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marina L.","family":"Kennerson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melissa J.","family":"Gordon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Annia K.","family":"Cherryson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Janet","family":"Nash","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tessy","family":"Bananis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"BFng0596101_CR1","doi-asserted-by":"publisher","first-page":"367","DOI":"10.1136\/bmj.2.5041.367","volume":"17","author":"L van Bogaert","year":"1957","unstructured":"van Bogaert, L. Familial ulcers, mutilating lesions of the extremities, and acro-osteolysis. Brit. Med. J. 17, 367\u2013371 (1957).","journal-title":"Brit. Med. J."},{"key":"BFng0596101_CR2","doi-asserted-by":"publisher","first-page":"2251","DOI":"10.1001\/jama.1939.02800220017006","volume":"112","author":"LM Tocantins","year":"1939","unstructured":"Tocantins, L.M. & Reimann, H.A. Perforating ulcers of feet with osseous atrophy. JAMA. 112, 2251\u20132255 (1939).","journal-title":"JAMA."},{"key":"BFng0596101_CR3","unstructured":"Dyck, P.J. Neuronal atrophy and degeneration predominantly affecting peripheral sensory and autonomic neurons, in Peripheral neuropathy(eds Dyck, P.J., Thomas, P.K., Lambert, E.H. & Bunge, R.) 1557\u20131559 (W.B. Saunders, Philadelphia, 1984)."},{"key":"BFng0596101_CR4","doi-asserted-by":"publisher","first-page":"237","DOI":"10.1136\/jnnp.14.4.237","volume":"14","author":"D Denny-Brown","year":"1951","unstructured":"Denny-Brown, D. Hereditary sensory radicular neuropathy. J. Neurol. Neurosurg. Psychiat. 14, 237\u2013252 (1951).","journal-title":"J. Neurol. Neurosurg. Psychiat."},{"key":"BFng0596101_CR5","doi-asserted-by":"publisher","first-page":"177","DOI":"10.1111\/j.1469-1809.1994.tb01887.x","volume":"58","author":"S Povey","year":"1994","unstructured":"Povey, S. et al. Report on the third international workshop on chromosome 9. Ann. Hum. Genet. 58, 177\u2013250 (1994).","journal-title":"Ann. Hum. Genet."},{"key":"BFng0596101_CR6","doi-asserted-by":"publisher","first-page":"347","DOI":"10.1111\/j.1469-1809.1995.tb00756.x","volume":"59","author":"MA Pericak-Vance","year":"1995","unstructured":"Pericak-Vance, M.A. et al. Report on the fourth international workshop on chromosome 9. Ann. Hum. Genet. 59, 347\u2013391 (1995).","journal-title":"Ann. Hum. Genet."},{"key":"BFng0596101_CR7","doi-asserted-by":"publisher","first-page":"1848","DOI":"10.1073\/pnas.91.5.1848","volume":"91","author":"G Del Sal","year":"1994","unstructured":"Del Sal, G. et al. Structure, function, and chromosome mapping of the growth-suppressing human homologue of the murine gas1 gene. Proc. Natl. Acad. Sci. U.S.A 91, 1848\u20131852 (1994).","journal-title":"Proc. Natl. Acad. Sci. U.S.A"},{"key":"BFng0596101_CR8","doi-asserted-by":"publisher","first-page":"288","DOI":"10.1038\/ng1292-288","volume":"2","author":"LJ Valentijn","year":"1992","unstructured":"Valentijn, L.J. et al. Identical point mutations of PMP-22 in trembler-J mouse and Charcot-Marie-Tooth disease type 1A. Nature Genet. 2, 288\u2013291 (1992).","journal-title":"Nature Genet."},{"key":"BFng0596101_CR9","doi-asserted-by":"publisher","first-page":"159","DOI":"10.1038\/ng0692-159","volume":"1","author":"PI Patel","year":"1992","unstructured":"Patel, P.I. et al. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nature Genet. 1, 159\u2013165 (1992).","journal-title":"Nature Genet."},{"key":"BFng0596101_CR10","doi-asserted-by":"publisher","first-page":"730","DOI":"10.1016\/0888-7543(95)80019-I","volume":"25","author":"SA Slaugenhaupt","year":"1995","unstructured":"Slaugenhaupt, S.A. et al. The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene. Genomics. 25, 730\u2013732 (1995).","journal-title":"Genomics."},{"key":"BFng0596101_CR11","doi-asserted-by":"publisher","first-page":"538","DOI":"10.1016\/0888-7543(95)80055-Q","volume":"25","author":"A Nakagawara","year":"1995","unstructured":"Nakagawara, A. et al. Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2). Genomics. 25, 538\u2013546 (1995).","journal-title":"Genomics."},{"key":"BFng0596101_CR12","doi-asserted-by":"publisher","first-page":"160","DOI":"10.1038\/ng0693-160","volume":"4","author":"A Blumenfeld","year":"1993","unstructured":"Blumenfeld, A. et al. Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nature Genet. 4, 160\u2013164 (1993).","journal-title":"Nature Genet."},{"key":"BFng0596101_CR13","doi-asserted-by":"publisher","first-page":"3","DOI":"10.1111\/j.1750-3639.1994.tb00806.x","volume":"4","author":"A Aguzzi","year":"1994","unstructured":"Aguzzi, A., Brandner, S., Sure, U., Ruedi, D. & Isenmann, S. Transgenic and knock-out mice: models of neurological disease. Brain Path. 4, 3\u201320 (1994).","journal-title":"Brain Path."},{"key":"BFng0596101_CR14","doi-asserted-by":"publisher","first-page":"42","DOI":"10.1016\/0959-4388(95)80085-9","volume":"5","author":"I Silos-Santiago","year":"1995","unstructured":"Silos-Santiago, I., Greenlund, L.J., Johnson, E.M. & Snider, W.D. Molecular genetics of neuronal survival. Curr. Opin. Neurobiol. 5, 42\u201349 (1995).","journal-title":"Curr. Opin. Neurobiol."},{"key":"BFng0596101_CR15","doi-asserted-by":"publisher","first-page":"59","DOI":"10.1038\/362059a0","volume":"362","author":"DR Rosen","year":"1993","unstructured":"Rosen, D.R. et al. Mutations in Cu\/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 362, 59\u201362 (1993).","journal-title":"Nature."},{"key":"BFng0596101_CR16","doi-asserted-by":"publisher","first-page":"2036","DOI":"10.1096\/fasebj.3.9.2568302","volume":"3","author":"JF Gusella","year":"1989","unstructured":"Gusella, J.F. Location cloning strategy for characterizing genetic defects in Huntington's disease and Alzheimer's disease. FASEB 3, 2036\u20132041 (1989).","journal-title":"FASEB"},{"key":"BFng0596101_CR17","doi-asserted-by":"publisher","first-page":"347","DOI":"10.1038\/ng0495-347","volume":"9","author":"FS Collins","year":"1995","unstructured":"Collins, F.S. Positional cloning moves from perditional to traditional. Nature Genet. 9, 347\u2013350 (1995).","journal-title":"Nature Genet."},{"key":"BFng0596101_CR18","first-page":"434","volume":"1","author":"M Jackson","year":"1949","unstructured":"Jackson, M. Familial lumbo-sacral syringomyelia and the significance of developmental errors of the spinal cord and column. Med. J. Aust. 1, 434\u2013439 (1949).","journal-title":"Med. J. Aust."},{"key":"BFng0596101_CR19","unstructured":"Wallace, D.C. Hereditary sensory radicular neuropathy. Archdall Medical Monograph 8 (Australasian Medical Publishing Co. Ltd., Sydney, 1970)."},{"key":"BFng0596101_CR20","first-page":"756","volume":"42","author":"LR Griffiths","year":"1988","unstructured":"Griffiths, L.R., Zwi, M.B., Mcleod, J.G. & Nicholson, G.A. Chromosome 1 linkage studies in Charcot-Marie-Tooth neuropathy. Am. J. Hum. Genet. 42, 756\u2013771 (1988).","journal-title":"Am. J. Hum. Genet."},{"key":"BFng0596101_CR21","doi-asserted-by":"publisher","first-page":"246","DOI":"10.1038\/ng0694supp-246","volume":"7","author":"G Gyapay","year":"1994","unstructured":"Gyapay, G. et al. The 1993-94 G\u00e9n\u00e9thon human genetic linkage map. Nature Genet. 7, 246\u2013339 (1994).","journal-title":"Nature Genet."},{"key":"BFng0596101_CR22","doi-asserted-by":"publisher","first-page":"203","DOI":"10.1006\/geno.1994.1049","volume":"19","author":"J Attwood","year":"1994","unstructured":"Attwood, J. et al. CEPH consortium map of chromosome 9. Genomics. 19, 203\u2013214 (1994).","journal-title":"Genomics."},{"key":"BFng0596101_CR23","doi-asserted-by":"publisher","first-page":"3443","DOI":"10.1073\/pnas.81.11.3443","volume":"81","author":"GM Lathrop","year":"1984","unstructured":"Lathrop, G.M., Lalouel, J.M., Julien, C. & Ott, J. Strategies for multilocus linkage analysis in humans. Proc. Natl. Acad. Sci. USA 81, 3443\u20133446 (1984).","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"BFng0596101_CR24","doi-asserted-by":"publisher","first-page":"356","DOI":"10.1159\/000132186","volume":"40","author":"PM Conneally","year":"1985","unstructured":"Conneally, P.M. et al. Report of the committee on methods of linkage analysis and reporting. Cytogenet. Cell Genet. 40, 356\u2013359 (1985).","journal-title":"Cytogenet. Cell Genet."}],"container-title":["Nature Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.nature.com\/articles\/ng0596-101","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/ng0596-101.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/ng0596-101.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,18]],"date-time":"2023-05-18T20:36:11Z","timestamp":1684442171000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/ng0596-101"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,5]]},"references-count":24,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1996,5]]}},"alternative-id":["BFng0596101"],"URL":"https:\/\/doi.org\/10.1038\/ng0596-101","relation":{},"ISSN":["1061-4036","1546-1718"],"issn-type":[{"value":"1061-4036","type":"print"},{"value":"1546-1718","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,5]]}}}