P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome -: art. no. e86
P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome -: art. no. e86
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DOI：
10.1136/jmg.2003.014902
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发表时间：
2004-06-01
影响因子：
4
通讯作者：
Brilliant, MH
中科院分区：
文献类型：
--
作者：
Garrison, NA;Yi, Z;Brilliant, MH
METHODS Patients All patients had OCA plus some suggestion of HPS or an HPS-related syndrome. Each was enrolled in a protocol approved by an NIH institutional review board and written informed consent was obtained from each patient or their parents.
