Genetic analysis of 100 consanguineous families to identify the molecular cause of mendelian visual impairment

被引：0
|
作者：
Ansar, M. [1 ]
Makrythanasis, P. [1 ,2 ]
Batool, N. [1 ]
Shaikh, H. [3 ]
Gul, K. [4 ]
Khan, A. A. [3 ]
Paracha, S. A. [5 ]
Khan, J. [5 ]
Qureshi, S. [4 ]
Imtiaz, S. [4 ]
Waryah, Y. M. [3 ]
Falconnet, E. [1 ]
Ribaux, P. G. [1 ]
Guipponi, M. [1 ,2 ]
Iqbal, Z. [6 ]
Borel, C. [1 ]
Santoni, F. A. [1 ,2 ]
Ahmed, J. [5 ]
Waryah, A. M. [3 ]
Sarwar, M. T. [5 ]
Antonarakis, S. E. [1 ,2 ,7 ]
机构：
[1] Univ Geneva, Dept Genet Med & Dev, Geneva, Switzerland
[2] Univ Hosp Geneva, Serv Genet Med, Geneva, Switzerland
[3] Liaquat Univ Med & Hlth Sci, Mol Biol & Genet Dept, Med Res Ctr, Jamshoro, Pakistan
[4] Univ Karachi, Dept Genet, Karachi, Pakistan
[5] Khyber Med Univ, IBMS, Peshawar, Pakistan
[6] Oslo Univ Hosp, Dept Neurol, Oslo, Norway
[7] iGE3, Geneva, Switzerland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P02.10B
引用
收藏
页码：174 / 174
页数：1
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