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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
Clinical features of DFNA5.
De Leenheer EM, van Zuijlen DA, Van Laer L, Van Camp G, Huygen PL, Huizing EH, Cremers CW. De Leenheer EM, et al. Among authors: huizing eh. Adv Otorhinolaryngol. 2002;61:53-9. doi: 10.1159/000066800. Adv Otorhinolaryngol. 2002. PMID: 12408063 No abstract available.
139 results