Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor (Q24312911)
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(P577) Friday, April 17, 1998

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(P1476) "Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor" (language: en)

(P2093) P A Frändberg
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M Doufexis
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S Kapas
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V Chhájlani
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(P356) 10.1006/BBRC.1998.8459
(P698) 9571181
(P3181) 948341
(P5875) 13709691