The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene (Q74153064)
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scientific article published on 01 July 2001
Language | Label | Description | Also known as |
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English | The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene |
scientific article published on 01 July 2001 |
Statements
The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene (English)
Olivares C
González P
Morandini R