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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: van de heyning p, van zuijlen d, van camp g. Nat Genet. 1998 Oct;20(2):194-7. doi: 10.1038/2503. Nat Genet. 1998. PMID: 9771715
Maternally inherited hearing impairment.
Van Camp G, Smith RJ. Van Camp G, et al. Clin Genet. 2000 Jun;57(6):409-14. doi: 10.1034/j.1399-0004.2000.570601.x. Clin Genet. 2000. PMID: 10905659 Review.
Is DFNA5 a susceptibility gene for age-related hearing impairment?
Van Laer L, DeStefano AL, Myers RH, Flothmann K, Thys S, Fransen E, Gates GA, Van Camp G, Baldwin CT. Van Laer L, et al. Among authors: van camp g. Eur J Hum Genet. 2002 Dec;10(12):883-6. doi: 10.1038/sj.ejhg.5200878. Eur J Hum Genet. 2002. PMID: 12461698
Nonsyndromic hearing loss.
Van Laer L, Cryns K, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: van camp g. Ear Hear. 2003 Aug;24(4):275-88. doi: 10.1097/01.AUD.0000079805.04016.03. Ear Hear. 2003. PMID: 12923419 Review.
DFNA5: hearing impairment exon instead of hearing impairment gene?
Van Laer L, Vrijens K, Thys S, Van Tendeloo VF, Smith RJ, Van Bockstaele DR, Timmermans JP, Van Camp G. Van Laer L, et al. Among authors: van tendeloo vf, van bockstaele dr, van camp g. J Med Genet. 2004 Jun;41(6):401-6. doi: 10.1136/jmg.2003.015073. J Med Genet. 2004. PMID: 15173223 Free PMC article.
552 results