In-depth characterization of mutations causing axonal recessive peripheral neuropathy with neuromyotonia (NMAN): the structure gives a HINT

被引：0
|
作者：
Amor-Barris, Silvia [1 ,2 ]
Lazar, Tamas [3 ,4 ]
Peeters, Kristien [1 ,2 ]
Wodak, Shoshana [3 ,4 ]
Jordanova, Albena [1 ,2 ,5 ]
机构：
[1] VIB Ctr Mol Neurol, Antwerp, Belgium
[2] Univ Antwerp, Antwerp, Belgium
[3] VIB Ctr Struct Biol, Brussels, Belgium
[4] Vrije Univ Brussel, Brussels, Belgium
[5] Med Univ Sofia, Sofia, Bulgaria
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2022年 / 30卷 / SUPPL 1期
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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：
P10.012.D
引用
收藏
页码：309 / 309
页数：1
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