Absence of AGG interruptions is a risk factor for a full mutation expansion among ethnically diverse FMR1 premutation carriers

被引：0
|
作者：
Domniz, N. [1 ]
Ries-Levavi, L. [1 ]
Cohen, Y. [1 ]
Haham, L. Marom [1 ]
Berkenstadt, M. [1 ]
Pras, E. [1 ]
Glicksman, A. [2 ]
Tortora, N. [2 ]
Latham, G. J. [3 ]
Hadd, A. G. [3 ]
Nolin, S. L. [2 ]
Elizur, S. [1 ]
机构：
[1] Sheba Med Ctr, Ramat Gan, Israel
[2] New York State Inst Basic Res Dev Disabil, New York, NY USA
[3] Asuragen, Austin, TX USA
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27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：
P01.28D
引用
收藏
页码：1186 / 1187
页数：2
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