Open AccessDFNA37 (autosomal dominant non-syndromic hearing loss 37) is caused by COL11A1 variants – confirmatory evidence by a novel splicing variant
Author(s) -
Thore Schade-Mann,
Barbara Vona,
Anke Tropitzsch,
Fritz Schneider,
Manfred Müller,
Saskia Biskup,
Hubert Löwenheim
Publication year - 2020
Publication title -
laryngo-, rhino-, otologie
Language(s) - English
Resource type - Conference proceedings
eISSN - 1438-8685
pISSN - 0935-8943
DOI - 10.1055/s-0040-1711065
Subject(s) - hearing loss , genetics , rna splicing , gene , biology , audiology , medicine , rna