Additional file 10: of Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Autor:	Lewis, Morag, Nolan, Lisa, Cadge, Barbara, Matthews, Lois, Schulte, Bradley, Dubno, Judy, Steel, Karen, Dawson, Sally
Rok vydání:	2018
DOI:	10.6084/m9.figshare.7047068
Popis:	Table S6. listing individuals homozygous for very rare variants in any gene. (DOCX 15 kb)
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eb71d1f1fd05a6f55ed30f89d85882e Zobrazit plný text záznamu