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Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort.
Carvalho, Simone da Costa E Silva; Grangeiro, Carlos Henrique Paiva; Picanço-Albuquerque, Clarissa Gondim; Dos Anjos, Thaís Oliveira; De Molfetta, Greice Andreotti; Silva, Wilson Araujo; Ferraz, Victor Evangelista de Faria.
Afiliación
  • Carvalho SDCES; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
  • Grangeiro CHP; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
  • Picanço-Albuquerque CG; Medical Genetics Service of the University Hospital of the Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
  • Dos Anjos TO; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
  • De Molfetta GA; Medical Genetics Service of the University Hospital of the Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
  • Silva WA; Center for Medical Genomics at University Hospital of the Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
  • Ferraz VEF; Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil.
BMC Res Notes ; 11(1): 546, 2018 Aug 02.
Article en En | MEDLINE | ID: mdl-30068397

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transportadores de Sulfato / Pérdida Auditiva Sensorineural / Mutación Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: America do sul / Brasil Idioma: En Revista: BMC Res Notes Año: 2018 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transportadores de Sulfato / Pérdida Auditiva Sensorineural / Mutación Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: America do sul / Brasil Idioma: En Revista: BMC Res Notes Año: 2018 Tipo del documento: Article País de afiliación: Brasil
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