<i>ATP1A1 de novo</i> Mutation-Related Disorders: Clinical and Genetic Features.

Lin, Zehong; Li, Jinliang; Ji, Taoyun; Wu, Ye; Gao, Kai; Jiang, Yuwu

ATP1A1 de novo Mutation-Related Disorders: Clinical and Genetic Features.

Lin, Zehong; Li, Jinliang; Ji, Taoyun; Wu, Ye; Gao, Kai; Jiang, Yuwu.

Afiliación

Lin Z; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Li J; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Ji T; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Wu Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Gao K; Department of Pediatrics, Peking University First Hospital, Beijing, China.
Jiang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.

Front Pediatr ; 9: 657256, 2021.

Article en En | MEDLINE | ID: mdl-33968856

Palabras clave

ATP1A1 gene; developmental delay; epilepsy; genotype-phenotype correlations; hypomagnesemia

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Pediatr Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

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