Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy-Reference-Cited by-同舟云学术

Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy

Author:

Dai Yi¹,Liang Shengran²,Dong Xue³,Zhao Yanhuan¹,Ren Haitao¹,Guan Yuzhou¹,Yin Haifang³,Li Chen⁴,Chen Lin¹,Cui Liying¹⁵,Banerjee Santasree⁴^ORCID

Affiliation:

1. Department of Neurology; Peking Union Medical College Hospital; Chinese Academy of Medical Sciences; Beijing China

2. School of Life Science and Biopharmaceuticals; Guangdong Pharmaceutical University; Guangzhou China

3. Department of Cell Biology; Tianjin Medical University; Tianjin China

4. Department of Cell Biology and Medical Genetics; School of Medicine; Zhejiang University; Hangzhou China

5. Neurosciences Center; Chinese Academy of Medical Sciences; Beijing China

Funder

Chinese National Basic Research Program

Chinese Academy of Medical Sciences

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

Reference27 articles.

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