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DFNA44 - Humpath.com - Human pathology

Home > E. Pathology by systems > Nervous system > Sensorial system > Ears > DFNA44

DFNA44

Tuesday 5 July 2011

The autosomal dominant progressive hearing loss designated DFNA44 is caused by a mutation in the CCDC50 gene (MIM.611051), which encodes an effector of epidermal growth factor-mediated cell signaling.

See also

- DFNAs