Review for "A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients"

2019 ◽  
Keyword(s):  
Muscular Dystrophy ◽  
Splice Site ◽  
Congenital Muscular Dystrophy ◽  
Splice Site Mutation ◽  
Chinese Patients ◽  
Site Mutation ◽  
Common Cause ◽  
I Gene

A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients

2020 ◽  
Vol 97 (5) ◽  
pp. 789-790
Author(s):  
Danyu Song ◽  
Xiaona Fu ◽  
Lin Ge ◽  
Xingzhi Chang ◽  
Cuijie Wei ◽  
...  
Keyword(s):  
Muscular Dystrophy ◽  
Splice Site ◽  
Congenital Muscular Dystrophy ◽  
Splice Site Mutation ◽  
Chinese Patients ◽  
Site Mutation ◽  
Common Cause
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