Corrigendum to 'A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss' [Biochem. Biophys. Res. Commun. 396 (2010) 626–630]

Subjects

Subjects :

Genetics
Hearing loss
Biophysics
medicine
Cell Biology
Biology
medicine.symptom
Molecular Biology
Biochemistry
Gene
Non syndromic
Frameshift mutation

Details

ISSN :

0006291X

Volume :

398

Database :

OpenAIRE

Journal :

Biochemical and Biophysical Research Communications

Accession number :

edsair.doi...........1c53702aeb22c5969b6d7c8888326311

Full Text :

https://doi.org/10.1016/j.bbrc.2010.06.061