Phenotypic and Molecular Characterization of Cockayne Syndrome; A Spotlight to Mild Cases

被引：0
|
作者：
Yesil, G. [1 ]
Akyuz, E. [1 ]
Gunes, N. [2 ]
Lessel, D. [3 ]
Kubisch, C. [3 ]
Tuysuz, B. [2 ]
机构：
[1] Bezmialem Vakif Univ, Dept Med Genet, Istanbul, Turkey
[2] IU Cerrahpasa Med Fac, Dept Pediat Genet, Istanbul, Turkey
[3] Ulm Univ, Inst Human Genet, Ulm, Germany
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：
P09.094B
引用
收藏
页码：406 / 407
页数：2
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