Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future.

Acharya, Anushree; Schrauwen, Isabelle; Leal, Suzanne M

Acharya, Anushree; Schrauwen, Isabelle; Leal, Suzanne M.

Acharya A; Center for Statistical Genetics, Gertrude H. Sergievsky Center, Columbia University Medical Center, New York, NY, USA.
Schrauwen I; Department of Neurology, Columbia University Medical Center, New York, NY, USA.
Leal SM; Center for Statistical Genetics, Gertrude H. Sergievsky Center, Columbia University Medical Center, New York, NY, USA.

Hum Genet ; 141(3-4): 413-430, 2022 Apr.

Article en En | MEDLINE | ID: mdl-34291353

Asunto(s)

Sordera; Pérdida Auditiva; Consanguinidad; Sordera/genética; Genes Recesivos; Pérdida Auditiva/genética; Humanos; Linaje

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sordera / Pérdida Auditiva Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

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