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Hypopigmentation in Hermansky-Pudlak syndrome
期刊名称:J Dermatol
时间:2012.12.24
页码:1-5
相关项目:基于核心家系的外显子组测序鉴定眼皮肤白化病致病基因
作者:
Wei AH|He X|Li W|
同期刊论文项目
基于核心家系的外显子组测序鉴定眼皮肤白化病致病基因
期刊论文 24
同项目期刊论文
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A comprehensive study of oculocutaneous albinism type 1 reveals three previously unidentified allele
Increasing the complexity: new genes and new types of albinism.
The BLOS1 interacting protein KXD1 is involved in the biogenesis of lysosome-related organelles.
Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.
Exome sequencing identifies SLC24A5 as a candidate gene for non-syndromic oculocutaneous albinism
Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and pathogenesis.
Hypopigmentation in Hermansky-Pudlak syndrome.
Genetic analyses of Chinese patients with digenic oculocutaneous albinism.
Hermansky-Pudlak syndrome: pigmentary and non-pigmentary defects and their pathogenesis.