2. Academic Validation
  3. The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene

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
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