The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene

  • J Invest Dermatol. 2001 Jul;117(1):156-8. doi: 10.1046/j.0022-202x.2001.01393.x.
C Jiménez-Cervantes ,  C Olivares ,  P González ,  R Morandini ,  G Ghanem ,  J C García-Borrón
PMID: 11442765 DOI: 10.1046/j.0022-202x.2001.01393.x