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Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation.
Hildebrand, M S; Thorne, N P; Bromhead, C J; Kahrizi, K; Webster, J A; Fattahi, Z; Bataejad, M; Kimberling, W J; Stephan, D; Najmabadi, H; Bahlo, M; Smith, R J H.
Affiliation
  • Hildebrand MS; Department of Otolaryngology, University of Iowa, Iowa City, IA, USA.
Clin Genet ; 77(6): 563-71, 2010 Jun.
Article in En | MEDLINE | ID: mdl-20132242
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myosins / Mutation, Missense / Hearing Loss Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Clin Genet Year: 2010 Document type: Article Affiliation country: United States Country of publication: Denmark
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myosins / Mutation, Missense / Hearing Loss Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Clin Genet Year: 2010 Document type: Article Affiliation country: United States Country of publication: Denmark