Figure 1 of
Mendoza-Reinoso, Mol Vis 2012; 18:2067-2075.
Figure 1.
Novel mutation Gly326Ser caused by a transition G→A in nucleotide
MYOC
976 changing codon GGT (Gly) to AGT (Ser). Found in case G62 and two of his first and second degree POAG affected relatives plus a younger relative with OHT.