Prevalence of genetically confirmed skeletal muscle channelopathies in the era of next generation sequencing-Reference-Cited by-同舟云学术

Prevalence of genetically confirmed skeletal muscle channelopathies in the era of next generation sequencing

Published:2023-03 Issue:3 Volume:33 Page:270-273
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Vivekanandam Vinojini^ORCID,Jaibaji Rawan,Sud Richa,Ellmers Rebecca,Skorupinska Iwona,Germaine Louise,James Natalie,Holmes Sarah,Mannikko Roope,Jayaseelan Dipa,Hanna Michael G

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference12 articles.

1. Skeletal Muscle Channelopathies;Vivekanandam;Neurol Clin,2020

2. Prevalence study of genetically defined skeletal muscle channelopathies in England;Horga;Neurology,2013

3. Translating genetic and functional data into clinical practice: a series of 223 families with myotonia;Suetterlin;Brain,2021

4. Andersen–Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity;Vivekanandam;Brain,2022

5. Population and household estimates, England and Wales - Office for National Statistics;Census,2022

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Diverse biophysical mechanisms in voltage‐gated sodium channel Na_v1.4 variants associated with myotonia;The FASEB Journal;2024-08-16

2. Myotone Dystrophien, nichtdystrophe Myotonien und periodische Paralysen;DGNeurologie;2024-04-18

3. Pediatric neuromuscular channelopathies;Handbook of Clinical Neurology;2024

4. A retrospective study of accuracy and usefulness of electrophysiological exercise tests;Journal of Neurology;2023-12-06

5. Muscle channelopathies: A review;Annals of the Child Neurology Society;2023-10-10