Novel missense mutation in exon 11 of LHCGR. (A) Chromatogram from one of two samples heterozygous for a novel C->T (Arg->Stop) missense mutation in codon 479 (exon 11) of LHCGR. (B) Chromatogram from a sample homozygous for 'C' at the same site.
Haasl et al. BMC Medical Genetics 2008 9:37 doi:10.1186/1471-2350-9-37