Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy.

Xia, Yu; Feng, Yijie; Xu, Lu; Chen, Xiaoyang; Gao, Feng; Mao, Shanshan

Xia, Yu; Feng, Yijie; Xu, Lu; Chen, Xiaoyang; Gao, Feng; Mao, Shanshan.

Afiliación

Xia Y; National Clinical Research Center for Child Health, Department of Neurology, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Feng Y; National Clinical Research Center for Child Health, Department of Neurology, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xu L; National Clinical Research Center for Child Health, Department of Neurology, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Chen X; National Clinical Research Center for Child Health, Department of Developmental and Behavioral Pediatrics, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Gao F; National Clinical Research Center for Child Health, Department of Neurology, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Mao S; National Clinical Research Center for Child Health, Department of Neurology, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Front Genet ; 12: 684042, 2021.

Article en En | MEDLINE | ID: mdl-34140971

Palabras clave

Duchenne muscular dystrophy; MLPA; Nusinersen (Spinraza); spinal muscular atrophy; synchronous diseases; whole-exome sequencing

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

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