Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects

Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects

Abstract Background Mutations in the SLC26A4 gene are associated with Pendred syndrome and autosomal recessive non-syndromic deafness (DFNB4). Both disorders have similar audiologic characteristics: bilateral hearing loss, often severe or profound, which may be associated with abnormalities of the i...

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Main Authors: Renata Watanabe Nonose (Author), Karina Lezirovitz (Author), Maria Teresa Balester de Mello Auricchio (Author), Ana Carla Batissoco (Author), Guilherme Lopes Yamamoto (Author), Regina Célia Mingroni-Netto (Author)
Format: Book
Published: BMC, 2018-05-01T00:00:00Z.
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3rd Floor Main Library

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