Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4-Reference-Cited by-同舟云学术

Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

Published:2001-11 Issue:5 Volume:69 Page:981-988
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Newton J.M.,Cohen-Barak Orit,Hagiwara Nobuko,Gardner John M.,Davisson Muriel T.,King Richard A.,Brilliant Murray H.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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4. Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka;Fukamachi;Nat Genet,2001

5. The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes;Gardner;Science,1992

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