Neurodegenerative Disorder Related to AIMP1/p43 Mutation Is Not a PMLD

被引：17
|
作者：
Boespflug-Tanguy, Odile [1 ,2 ,3 ]
Aubourg, Patrick [4 ]
Dorboz, Imen [3 ]
Begou, Melina [3 ,5 ]
Giraud, Genevieve [3 ,5 ]
Sarret, Catherine [3 ,5 ,6 ]
Vaurs-Barriere, Catherine [3 ,5 ]
机构：
[1] Robert Debre Univ Hosp, APHP, Reference Ctr Rare Dis Leukodystrophies, Child Neurol & Metab Disorders Dept, F-75935 Paris, France
[2] Univ Paris 07, F-75013 Paris, France
[3] Inst Natl Sante & Rech Med, UMR 931, CNRS 6247, Genet Reprod & Dev Med Sch, F-63000 Clermont Ferrand, France
[4] Pediat Neurol St Vincent de Paul Hosp, APHP, Reference Ctr Rare Dis Leukodystrophies, F-75014 Paris, France
[5] Auvergne Univ Med Sch, F-63000 Clermont Ferrand, France
[6] Clermont Ferrand Univ Hosp, Dept Paediat, F-63000 Clermont Ferrand, France
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2011年 / 88卷 / 03期
关键词：
MERZBACHER-LIKE-DISEASE;
D O I：
10.1016/j.ajhg.2010.12.015
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：392 / 393
页数：2
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