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Table 4 Heterozygous mutations of SMN, NAIP and GTF2H2 genes among children

From: New multiplex real-time PCR approach to detect gene mutations for spinal muscular atrophy

 

SMN

NAIP

GTF2H2

Exon7

Exon4

Exon5

Exon10

SMA

0

0

0

0

DMD/BMD

38

1

1

0

ME

1

0

0

0

CMT

0

0

0

0

Normal

23

7

3

4