Artículos de revistas
Molecular Genetics Of Non-syndromic Deafness [genética Molecular Da Deficiência Auditiva Não-sindrômica]
Registro en:
Revista Brasileira De Otorrinolaringologia. , v. 71, n. 2, p. 216 - 223, 2005.
347299
2-s2.0-20344382047
Autor
Piatto V.B.
Nascimento E.C.T.
Alexandrino F.
Oliveira C.A.
Lopes A.C.P.
Sartorato E.L.
Maniglia J.V.
Institución
Resumen
One in every 1.000 newborn suffers from congenital hearing impairment. More than 60% of the congenital cases are caused by genetic factors. In most cases, hearing loss is a multifactorial disorder caused by both genetic and environmental factors. Molecular genetics of deafness has experienced remarkable progress in the last decade. Genes responsible for hereditary hearing impairment are being mapped and cloned progressively. 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