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

页码：174 / 174

页数：1

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