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

页码：S112 / S112

页数：1

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