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
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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

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

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