Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review

Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review

X-linked deafness (DFNX) is estimated to account for up to 2% of cases of hereditary hearing loss and occurs in both syndromic and non-syndromic forms. <i>POU3F4</i> is the gene most commonly associated with X-linked deafness (DFNX2, DFN3) and accounts for about 50% of the cases of X-lin...

Full description

Bibliographic Details
Main Authors: Emanuele Bernardinelli, Florian Huber, Sebastian Roesch, Silvia Dossena
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:Biomedicines
Subjects:
POU3F4
X-linked deafness
transcription factor
hearing loss
gene variants
Online Access:https://www.mdpi.com/2227-9059/11/6/1695

Similar Items

Similar Items