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Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor.

Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Biochemical and Biophysical Research Communications Pubmed

Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor.

Frändberg, P A; Doufexis, M; Kapas, S; Chhájlani, V
Biochemical and Biophysical Research Communications , Volume 245 (2): -487 – Jun 2, 1998
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ISSN
0006-291X
DOI
10.1006/bbrc.1998.8459
pmid
9571181

Abstract

Journal

Biochemical and Biophysical Research Communications – Pubmed

Published: Jun 2, 1998

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