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A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy.
Matsunaga, T; Mutai, H; Kunishima, S; Namba, K; Morimoto, N; Shinjo, Y; Arimoto, Y; Kataoka, Y; Shintani, T; Morita, N; Sugiuchi, T; Masuda, S; Nakano, A; Taiji, H; Kaga, K.
Affiliation
  • Matsunaga T; Laboratory of Auditory Disorders, National Institute of Sensory Organs, National Tokyo Medical Center, Tokyo, Japan.
Clin Genet ; 82(5): 425-32, 2012 Nov.
Article in En | MEDLINE | ID: mdl-22575033
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Founder Effect / Genetic Association Studies / Hearing Loss, Central / Membrane Proteins Type of study: Prevalence_studies / Risk_factors_studies Limits: Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Genet Year: 2012 Document type: Article Affiliation country:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Founder Effect / Genetic Association Studies / Hearing Loss, Central / Membrane Proteins Type of study: Prevalence_studies / Risk_factors_studies Limits: Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Clin Genet Year: 2012 Document type: Article Affiliation country: