{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,17]],"date-time":"2023-10-17T19:25:58Z","timestamp":1697570758976},"reference-count":24,"publisher":"Springer Science and Business Media LLC","issue":"9","license":[{"start":{"date-parts":[[2001,9,1]],"date-time":"2001-09-01T00:00:00Z","timestamp":999302400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Hum Genet"],"published-print":{"date-parts":[[2001,9]]},"DOI":"10.1038\/sj.ejhg.5200707","type":"journal-article","created":{"date-parts":[[2002,9,18]],"date-time":"2002-09-18T22:09:33Z","timestamp":1032386973000},"page":"667-671","source":"Crossref","is-referenced-by-count":11,"title":["Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26"],"prefix":"10.1038","volume":"9","author":[{"given":"Massimo","family":"Mangino","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elisabetta","family":"Flex","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesca","family":"Capon","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Federica","family":"Sangiuolo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Edoardo","family":"Carraro","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesca","family":"Gualandi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manuela","family":"Mazzoli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alessandro","family":"Martini","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giuseppe","family":"Novelli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bruno","family":"Dallapiccola","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2001,9,14]]},"reference":[{"key":"BF5200707_CR1","unstructured":"Cohen MM, Gorlin RJ: . Epidemiology, etiology and genetic patterns. In Gorlin RJ, Toriello HV, Cohen MM (eds) Hereditary hearing loss and its syndromes Oxford: Oxford University Press 1995 pp. 9\u201321"},{"key":"BF5200707_CR2","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1101\/gr.9.1.7","volume":"9","author":"BJ Keats","year":"1999","unstructured":"Keats BJ, Berlin CI . Genomics and hearing impairment Genome Res 1999 9: 7\u201316","journal-title":"Genome Res"},{"key":"BF5200707_CR3","first-page":"758","volume":"60","author":"G Van Camp","year":"1997","unstructured":"Van Camp G, Willems PJ, Smith RJ . Nonsyndromic hearing impairment: unparalleled heterogeneity Am J Hum Genet 1997 60: 758\u2013764","journal-title":"Am J Hum Genet"},{"key":"BF5200707_CR4","doi-asserted-by":"publisher","first-page":"143","DOI":"10.1038\/84758","volume":"27","author":"KP Steel","year":"2001","unstructured":"Steel KP, Kros CJ . A genetic approach to understanding auditory function Nat Genet 2001 27: 143\u2013149","journal-title":"Nat Genet"},{"key":"BF5200707_CR5","doi-asserted-by":"publisher","first-page":"560","DOI":"10.1038\/nm0598-560","volume":"4","author":"S Heller","year":"1998","unstructured":"Heller S, Hudspeth AJ . Two deaf mice, two deaf mice: murine candidate genes pinpoint the genetic bases of non-syndromic hearing loss in humans Nat Med 1998 4: 560\u2013561","journal-title":"Nat Med"},{"key":"BF5200707_CR6","first-page":"460","volume":"36","author":"GM Lathrop","year":"1984","unstructured":"Lathrop GM, Lalouel JM . Easy calculations of lod scores and genetic risks on small computers Am J Hum Genet 1984 36: 460\u2013465","journal-title":"Am J Hum Genet"},{"key":"BF5200707_CR7","doi-asserted-by":"publisher","first-page":"1047","DOI":"10.1093\/hmg\/5.7.1047","volume":"5","author":"EN Manolis","year":"1996","unstructured":"Manolis EN, Yandavi N, Nadol Jr JB et al. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13 Hum Mol Genet 1996 5: 1047\u20131050","journal-title":"Hum Mol Genet"},{"key":"BF5200707_CR8","doi-asserted-by":"publisher","first-page":"2159","DOI":"10.1093\/hmg\/4.11.2159","volume":"4","author":"G van Camp","year":"1995","unstructured":"van Camp G, Coucke P, Balemans W et al. Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15 Hum Mol Genet 1995 4: 2159\u20132163","journal-title":"Hum Mol Genet"},{"key":"BF5200707_CR9","doi-asserted-by":"publisher","first-page":"285","DOI":"10.1093\/hmg\/7.2.285","volume":"7","author":"MS Tomek","year":"1998","unstructured":"Tomek MS, Brown MR, Mani SR et al. Localization of a gene for otosclerosis to chromosome 15q25-q26 Hum Mol Genet 1998 7: 285\u2013290","journal-title":"Hum Mol Genet"},{"key":"BF5200707_CR10","doi-asserted-by":"publisher","first-page":"152","DOI":"10.1038\/380152a0","volume":"380","author":"C Dib","year":"1996","unstructured":"Dib C, Faure S, Fizames C et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites Nature 1996 380: 152\u2013154","journal-title":"Nature"},{"key":"BF5200707_CR11","doi-asserted-by":"publisher","first-page":"794","DOI":"10.1038\/359794a0","volume":"359","author":"J Weissenbach","year":"1992","unstructured":"Weissenbach J, Gyapay G, Dib C et al. A second-generation linkage map of the human genome Nature 1992 359: 794\u2013801","journal-title":"Nature"},{"key":"BF5200707_CR12","doi-asserted-by":"publisher","first-page":"246","DOI":"10.1038\/ng0694supp-246","volume":"7","author":"G Gyapay","year":"1994","unstructured":"Gyapay G, Morissette J, Vignal A et al. The 1993-94 Genethon human genetic linkage map Nat Genet 1994 7: 246\u2013339","journal-title":"Nat Genet"},{"key":"BF5200707_CR13","doi-asserted-by":"publisher","first-page":"402","DOI":"10.1038\/ng1295-402","volume":"11","author":"JR O'Connell","year":"1995","unstructured":"O'Connell JR, Weeks DE . The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance Nat Genet 1995 11: 402\u2013408","journal-title":"Nat Genet"},{"key":"BF5200707_CR14","doi-asserted-by":"publisher","first-page":"535","DOI":"10.1042\/bj3090535","volume":"309","author":"WB Valhmu","year":"1995","unstructured":"Valhmu WB, Palmer GD, Rivers PA et al. Structure of the human aggrecan gene: exon-intron organization and association with the protein domains Biochem J 1995 309: 535\u2013542","journal-title":"Biochem J"},{"key":"BF5200707_CR15","doi-asserted-by":"publisher","first-page":"13974","DOI":"10.1074\/jbc.272.21.13974","volume":"272","author":"KJ Doege","year":"1997","unstructured":"Doege KJ, Coulter SN, Meek LM, Maslen K, Wood JG . A human-specific polymorphism in the coding region of the aggrecan gene. Variable number of tandem repeats produce a range of core protein sizes in the general population J Biol Chem 1997 272: 13974\u201313979","journal-title":"J Biol Chem"},{"key":"BF5200707_CR16","doi-asserted-by":"publisher","first-page":"1015","DOI":"10.1136\/jmg.34.12.1015","volume":"34","author":"DA Campbell","year":"1997","unstructured":"Campbell DA, McHale DP, Brown KA et al. A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22 J Med Genet 1997 34: 1015\u20131017","journal-title":"J Med Genet"},{"key":"BF5200707_CR17","doi-asserted-by":"publisher","first-page":"188","DOI":"10.1038\/ng0697-188","volume":"16","author":"XZ Liu","year":"1997","unstructured":"Liu XZ, Walsh J, Mburu P et al. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness Nat Genet 1997 16: 188\u2013190","journal-title":"Nat Genet"},{"key":"BF5200707_CR18","doi-asserted-by":"publisher","first-page":"268","DOI":"10.1038\/ng1197-268","volume":"17","author":"XZ Liu","year":"1997","unstructured":"Liu XZ, Walsh J, Tamagawa Y et al. Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene Nat Genet 1997 17: 268\u2013269","journal-title":"Nat Genet"},{"key":"BF5200707_CR19","doi-asserted-by":"publisher","first-page":"191","DOI":"10.1038\/ng0697-191","volume":"16","author":"D Weil","year":"1997","unstructured":"Weil D, Kussel P, Blanchard S et al. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene Nat Genet 1997 16: 191\u2013193","journal-title":"Nat Genet"},{"key":"BF5200707_CR20","doi-asserted-by":"publisher","first-page":"16","DOI":"10.1038\/12612","volume":"23","author":"A Grifa","year":"1999","unstructured":"Grifa A, Wagner CA, D'Ambrosio L et al. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus Nat Genet 1999 23: 16\u201318","journal-title":"Nat Genet"},{"key":"BF5200707_CR21","doi-asserted-by":"publisher","first-page":"80","DOI":"10.1038\/387080a0","volume":"387","author":"DP Kelsell","year":"1997","unstructured":"Kelsell DP, Dunlop J, Stevens HP et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness Nature 1997 387: 80\u201383","journal-title":"Nature"},{"key":"BF5200707_CR22","doi-asserted-by":"publisher","first-page":"335","DOI":"10.3109\/03005369909090117","volume":"33","author":"SJ Bom","year":"1999","unstructured":"Bom SJ, Kunst HP, Huygen PL, Cremers FP, Cremers CW . Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes Br J Audiol 1999 33: 335\u2013348","journal-title":"Br J Audiol"},{"key":"BF5200707_CR23","doi-asserted-by":"publisher","first-page":"254","DOI":"10.1086\/316925","volume":"68","author":"CC Greene","year":"2001","unstructured":"Greene CC, McMillan PM, Barker SE et al. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24 Am J Hum Genet 2001 68: 254\u2013260","journal-title":"Am J Hum Genet"},{"key":"BF5200707_CR24","doi-asserted-by":"publisher","first-page":"431","DOI":"10.1038\/82558","volume":"26","author":"S Riazuddin","year":"2000","unstructured":"Riazuddin S, Castelein CM, Ahmed ZM et al. Dominant modifier DFNM1 suppresses recessive deafness DFNB26 Nat Genet 2000 26: 431\u2013434","journal-title":"Nat Genet"}],"container-title":["European Journal of Human Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.nature.com\/articles\/5200707.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/5200707","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/5200707.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,18]],"date-time":"2023-05-18T01:27:15Z","timestamp":1684373235000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/5200707"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2001,9]]},"references-count":24,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2001,9]]}},"alternative-id":["BF5200707"],"URL":"https:\/\/doi.org\/10.1038\/sj.ejhg.5200707","relation":{},"ISSN":["1018-4813","1476-5438"],"issn-type":[{"value":"1018-4813","type":"print"},{"value":"1476-5438","type":"electronic"}],"subject":[],"published":{"date-parts":[[2001,9]]}}}