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A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
Mujtaba, Ghulam; Schultz, Julie M; Imtiaz, Ayesha; Morell, Robert J; Friedman, Thomas B; Naz, Sadaf.
  • Mujtaba G; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
  • Schultz JM; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA Present address, GeneDx, Gaithersburg, Maryland, USA.
  • Imtiaz A; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
  • Morell RJ; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Friedman TB; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.
  • Naz S; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
J Med Genet ; 52(8): 548-52, 2015 Aug.
Article en En | MEDLINE | ID: mdl-25941349
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Proto-Oncogénicas c-met / Mutación Missense / Pérdida Auditiva Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Proto-Oncogénicas c-met / Mutación Missense / Pérdida Auditiva Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article