From: Mutation analysis of 419 family and prenatal diagnosis of 339 cases of spinal muscular atrophy in China
Changes of cDNA
Exon
Novel
c.21_22insA
1
Y
c.22dupA
N
c.56delT
c.683 T > A
5
c.689C > T
c.835G > C
7
c.836G > T
c.863G > T
8
c.840C > T
c.885 + 3A > T