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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