Author response for "Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by <scp>NGS</scp> gene panel and <scp>WES</scp>"
Dana Šafka Brožková(Charles University), Pavel Seeman, Zdeněk Čada(Charles University), Anna Uhrová Mészárosová(Charles University), Simona Poisson Marková(Charles University), Ján Jenčík(Charles University), Dagmar Ras̆ková(Gennet), Jana Laštůvková(Krajská Zdravotní)
Cited by 0
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