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. 2014 Apr 20;23(2):53–58. doi: 10.1297/cpe.23.53

Fig. 1.

Fig. 1.

Genetic analysis of the LH/CGR gene. The patient is heterozygous for a C to T transition at nucleotide c.1715. This mutation results in substitution of Val for Ala at codon 572 (p.A572V mutation). His parents are homozygous for the wild-type allele.