Nonsyndromic hearing impairment is associated with a mutation in DFNA5.
Van Laer L, Huizing EH, Verstreken M, van Zuijlen D, Wauters JG, Bossuyt PJ, Van de Heyning P, McGuirt WT, Smith RJ, Willems PJ, Legan PK, Richardson GP, Van Camp G.
Van Laer L, et al. Among authors: huizing eh.
Nat Genet. 1998 Oct;20(2):194-7. doi: 10.1038/2503.
Nat Genet. 1998.
PMID: 9771715