Spectrum of skeletal muscle channelopathies in a cohort of Inherited neuromuscular disorders

被引：0
|
作者：
Sidharth, S. [1 ]
Macken, W. [2 ,3 ]
Mishra, R. [1 ]
Reyaz, A. [1 ]
Ahmed, T. [1 ]
Bhatia, R. [1 ]
Pitceathly, R. [2 ,3 ]
Thangaraj, K. [4 ,5 ]
Srivastava, P. [1 ]
Hanna, M. [2 ,3 ]
Venugopalan, V. [1 ]
机构：
[1] All India Inst Med Sci, New Delhi, India
[2] UCL Queen Sq Inst Neurol, Dept Neuromuscular Dis, London, England
[3] Natl Hosp Neurol & Neurosurg, Queen Sq Ctr Neuromuscular Dis, NHS Highly Specialised Serv Rare Mitochondrial Di, London, England
[4] Ctr Cellular Mol Biol, Hyderabad, India
[5] Ctr DNA Fingerprinting & Diagnost, Hyderabad, India
来源：
NEUROMUSCULAR DISORDERS | 2023年 / 33卷
关键词：
D O I：
10.1016/j.nmd.2023.07.186
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P186
引用
收藏
页码：S112 / S112
页数：1
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