Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype.

被引：0
|
作者：
King, R
Pietsch, J
Fryer, JP
Savage, S
Brott, MJ
Russell-Eggitt, I
Summers, CG
Oetting, WS
机构：
[1] Univ Minnesota, Minneapolis, MN USA
[2] Great Ormond St Hosp Children, London WC1N 3JH, England
[3] Univ Minnesota, Inst Human Genet, Minneapolis, MN USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2202
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收藏
页码：544 / 544
页数：1
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