Your browser doesn't support javascript.
loading
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment.
Adadey, Samuel M; Schrauwen, Isabelle; Aboagye, Elvis Twumasi; Bharadwaj, Thashi; Esoh, Kevin K; Basit, Sulman; Acharya, Anushree; Nouel-Saied, Liz M; Liaqat, Khurram; Wonkam-Tingang, Edmond; Mowla, Shaheen; Awandare, Gordon A; Ahmad, Wasim; Leal, Suzanne M; Wonkam, Ambroise.
Afiliación
  • Adadey SM; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.
  • Schrauwen I; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Aboagye ET; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Centre, New York, NY, USA.
  • Bharadwaj T; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.
  • Esoh KK; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Centre, New York, NY, USA.
  • Basit S; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Acharya A; Center for Genetics and Inherited Diseases, Taibah University Al Madinah Al Munawarah, Al Munawarah, Saudi Arabia.
  • Nouel-Saied LM; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Centre, New York, NY, USA.
  • Liaqat K; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Centre, New York, NY, USA.
  • Wonkam-Tingang E; Faculty of Biological Sciences, Department of Biotechnology, Quaid-i-Azam University, Islamabad, Pakistan.
  • Mowla S; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Awandare GA; Division of Haematology, Faculty of Health Sciences, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Ahmad W; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.
  • Leal SM; Faculty of Biological Sciences, Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.
  • Wonkam A; Center for Statistical Genetics, Gertrude H. Sergievsky Center, and the Department of Neurology, Columbia University Medical Centre, New York, NY, USA. sml3@cumc.columbia.edu.
J Hum Genet ; 66(12): 1169-1175, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34226616

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Estudios de Asociación Genética / Miembro 2 de la Familia de Transportadores de Soluto 12 / Pérdida Auditiva / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Ghana

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Estudios de Asociación Genética / Miembro 2 de la Familia de Transportadores de Soluto 12 / Pérdida Auditiva / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Ghana