A synonymous substitution in the VMA21 gene cosegregating with a severe neonatal form of x-linked myopathy with excessive autophagy (XMEA)

被引：0
|
作者：
Blanco, Patricia [1 ]
Arrabal Fernandez, Luisa [2 ]
Fernandez Garcia, Miguel Angel [1 ]
Perin, Francesca [3 ]
机构：
[1] Grp Hlth Code, Area Neurolo, La Coruna, Spain
[2] Hosp Virgen Ias Nieves, Serv Neuropediat, Granada, Spain
[3] Hosp Virgen Ias Nieves, Unidad Cardiologia Pediat, Serv Pediat, Granada, Spain
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31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：
EP11.022
引用
收藏
页码：215 / 215
页数：1
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