[HTML][HTML] Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review
E Bernardinelli, F Huber, S Roesch, S Dossena - Biomedicines, 2023 - mdpi.com
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. POU3F4 is the gene …
hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene …
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.
E Bernardinelli, F Huber, S Roesch… - Biomedicines, 2023 - search.ebscohost.com
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. POU3F4 is the gene …
hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene …
[HTML][HTML] Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review
E Bernardinelli, F Huber, S Roesch, S Dossena - Biomedicines, 2023 - ncbi.nlm.nih.gov
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. POU3F4 is the gene …
hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene …
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review
E Bernardinelli, F Huber, S Roesch… - …, 2023 - pubmed.ncbi.nlm.nih.gov
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. POU3F4 is the gene …
hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene …
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.
E Bernardinelli, F Huber, S Roesch, S Dossena - Biomedicines, 2023 - europepmc.org
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. POU3F4 is the gene …
hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene …
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review
E Bernardinelli, F Huber, S Roesch… - Biomedicines, 2023 - search.proquest.com
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. POU3F4 is the gene …
hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene …