Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

1 October 2001

journal article
Published by Oxford University Press (OUP) in Human Molecular Genetics

Vol. 10 (22), 2509-2514
https://doi.org/10.1093/hmg/10.22.2509

Abstract

Read the full review for this F1000Prime recommended article: Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.

Keywords

NEUROBIOLOGY OF DISEASE & REGENERATION
SENSORY SYSTEMS
GENOMICS
MEDICAL GENETICS
KEY PAPER

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