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MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform.
Grati, M'hamed; Yan, Denise; Raval, Manmeet H; Walsh, Tom; Ma, Qi; Chakchouk, Imen; Kannan-Sundhari, Abhiraami; Mittal, Rahul; Masmoudi, Saber; Blanton, Susan H; Tekin, Mustafa; King, Mary-Claire; Yengo, Christopher M; Liu, Xue Zhong.
Afiliação
  • Grati M; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Yan D; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Raval MH; Department of Cellular and Molecular Physiology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania.
  • Walsh T; Departments of Medicine and Genome Sciences, University of Washington, Seattle, Washington.
  • Ma Q; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Chakchouk I; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Kannan-Sundhari A; Laboratoire Procédés de Criblage Moléculaire et Cellulaire, Centre de Biotechnologie de Sfax, Université de Sfax, Sfax, Tunisie.
  • Mittal R; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Masmoudi S; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Blanton SH; Laboratoire Procédés de Criblage Moléculaire et Cellulaire, Centre de Biotechnologie de Sfax, Université de Sfax, Sfax, Tunisie.
  • Tekin M; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • King MC; Dr. John T. Macdonald Foundation, Department of Human Genetics, and John P. Hussman Institute for Human Genomics, University of Miami, Miami, Florida.
  • Yengo CM; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida.
  • Liu XZ; Dr. John T. Macdonald Foundation, Department of Human Genetics, and John P. Hussman Institute for Human Genomics, University of Miami, Miami, Florida.
Hum Mutat ; 37(5): 481-7, 2016 May.
Article em En | MEDLINE | ID: mdl-26841241
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Caderinas / Cadeias Pesadas de Miosina / Polimorfismo de Nucleotídeo Único / Miosina Tipo III / Surdez Tipo de estudo: Etiology_studies Limite: Animals / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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XML
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Caderinas / Cadeias Pesadas de Miosina / Polimorfismo de Nucleotídeo Único / Miosina Tipo III / Surdez Tipo de estudo: Etiology_studies Limite: Animals / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article