The Pro162 Variant is a Loss-of-Function Mutation of the Human Melanocortin 1 Receptor Gene
- 1 July 2001
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 117 (1) , 156-158
- https://doi.org/10.1046/j.0022-202x.2001.01393.x
Abstract
No abstract availableKeywords
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