Fig. 2From: Delayed diagnosis of complex glycerol kinase deficiency in a Chinese male infant: a case reportResults of gene screening via multiplex PCR amplification and DHPLC analysis. a, b, and c demonstrate all exons of the DMD, GK, and NROB1 genes were heterozygous deletions in samples of this boy’s mother. While d, e, and f reveal deletions of DMD, GK, and NROB1 genes of this boyBack to article page