Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients
Simona Poisson Marková(Charles University), Pavel Seeman, Petra Laššuthová(Northwestern University), Daniel Groh, Anna Uhrová Mészárosová(Charles University), Jana Neupauerová(Charles University), Dana Šafka Brožková(Charles University), Gabriela Křečková(Gennet)
Cited by 17
Related Papers
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
|The American Journal of Human Genetics|2005|562
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene
|European Journal of Human Genetics|2008|53
Biallelic variants in <i>HPDL</i> cause pure and complicated hereditary spastic paraplegia
|Brain|2021|52