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Autor:
Franziska M. Häfner, Damina Balmer, Albert Schinzel, Thomas E. Linder, Allessandra Baumer, Thomas Spillmann, Ambar A. Salam, Suzanne M. Leal
Publikováno v:
The American Journal of Human Genetics. 66:1437-1442
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 autosomal dominant nonsyndromic hearing–loss loci have been mapped, and 11 genes have been isolated. In the majority of cases, autosomal dominant non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f6ee0fcd05a07982c0aa40e709951ba
https://doi.org/10.1086/302865
https://doi.org/10.1086/302865
