[Family genetic analysis of paternal Dystrophin gene mutations in a case of female Duchenne muscular dystrophy].

Mao, Y Y; Chen, Q; Zhang, X; Xu, K M; Gao, Z J; Zhang, P P

Mao, Y Y; Chen, Q; Zhang, X; Xu, K M; Gao, Z J; Zhang, P P.

Afiliação

Mao YY; Department of Neurology, Children's Hospital of Capital Institute of Pediatrics, Beijing 100020, China.
Chen Q; Department of Neurology, Children's Hospital of Capital Institute of Pediatrics, Beijing 100020, China.
Zhang X; Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Beijing 100730, China.
Xu KM; Department of Neurology, Children's Hospital of Capital Institute of Pediatrics, Beijing 100020, China.
Gao ZJ; Department of Neurology, Children's Hospital of Capital Institute of Pediatrics, Beijing 100020, China.
Zhang PP; Department of Neurology, Children's Hospital of Capital Institute of Pediatrics, Beijing 100020, China.

Zhonghua Yi Xue Za Zhi ; 101(48): 3973-3976, 2021 Dec 28.

Article em Zh | MEDLINE | ID: mdl-34955001

Assuntos

Distrofina; Distrofia Muscular de Duchenne; Distrofina/genética; Feminino; Testes Genéticos; Heterozigoto; Humanos; Distrofia Muscular de Duchenne/genética; Mutação; Linhagem; Gravidez

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofina / Distrofia Muscular de Duchenne Tipo de estudo: Prognostic_studies Limite: Female / Humans / Pregnancy Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Ano de publicação: 2021 Tipo de documento: Article

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