ℹ️
🇬🇧
Search
Search for publications relevant for "DFNB16"
DFNB16
Publication
Class
Person
Publication
Programmes
publication
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene
2019 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing
2020 |
First Faculty of Medicine, Second Faculty of Medicine