欢迎您!
东篱公司
退出
申报数据库
申报指南
立项数据库
成果数据库
期刊论文
会议论文
著 作
专 利
项目获奖数据库
位置:
成果数据库
>
期刊
> 期刊详情页
Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.
ISSN号:0022-202X
期刊名称:Journal of Investigative Dermatology
时间:2013.7
页码:1834-1840
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:
Liu, Xuan-Zhu|He, Xin|Yang, Lin|Wang, Yi|Zhou, Zhi-Yong|Zhang, Ming-Rong|Dai, Lan-Lan|Yang, Xiu-Min|Li, Wei|
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
Genetic analyses of Chinese patients with digenic oculocutaneous albinism
Increasing the complexity: new genes and new types of albinism
Genetic analyses of Chinese patients with compound oculocutaneous albinism
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.
Hypopigmentation in Hermansky-Pudlak syndrome
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.