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A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family.
Patel, Kunjan; Giese, Arnaud P; Grossheim, J M; Hegde, Rashmi S; Hegde, Rashima S; Delio, Maria; Samanich, Joy; Riazuddin, Saima; Frolenkov, Gregory I; Cai, Jinlu; Ahmed, Zubair M; Morrow, Bernice E.
Afiliación
  • Patel K; Department of Genetics, Albert Einstein College of Medicine, 1301 Morris Park Avenue, Bronx, New York, United States of America.
  • Giese AP; Department of Otorhinolaryngology Head & Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America.
  • Grossheim JM; Department of Physiology, College of Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
  • Hegde RS; Division of Developmental Biology, Cincinnati Children's Hospital Medical Centre Cincinnati, Ohio, United States of America.
  • Delio M; Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, New York, United States of America.
  • Samanich J; Department of Pediatrics (Clinical Genetics), Albert Einstein College of Medicine; Montefiore Medical Center, Bronx, New York, United States of America.
  • Riazuddin S; Department of Otorhinolaryngology Head & Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America.
  • Frolenkov GI; Department of Physiology, College of Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
  • Cai J; Department of Genetics, Albert Einstein College of Medicine, 1301 Morris Park Avenue, Bronx, New York, United States of America.
  • Ahmed ZM; Department of Otorhinolaryngology Head & Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland, United States of America.
  • Morrow BE; Department of Genetics, Albert Einstein College of Medicine, 1301 Morris Park Avenue, Bronx, New York, United States of America.
PLoS One ; 10(10): e0133082, 2015.
Article en En | MEDLINE | ID: mdl-26426422
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Linaje / Proteínas de Unión al Calcio / Hispánicos o Latinos / Mutación Missense / Pérdida Auditiva Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Animals / Child / Female / Humans / Infant / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Linaje / Proteínas de Unión al Calcio / Hispánicos o Latinos / Mutación Missense / Pérdida Auditiva Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Animals / Child / Female / Humans / Infant / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos