Fig. 2From: A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemiaMultiplex ligation-dependent probe amplification analysis of GLDC, AMT and GCSH genes. A heterozygous deletion of exon 3 in GLDC gene was detected in the proband (a) and his father (c), but not in his mother (b)Back to article page