Corrigendum to ‘Hypotonic Infant with PURA Syndrome-related Channelopathy Successfully Treated with Pyridostigmine’ Neuromuscular Disorders Volume 32, Issue 2, February 2022, Pages 166-169-Reference-Cited by-同舟云学术

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Corrigendum to ‘Hypotonic Infant with PURA Syndrome-related Channelopathy Successfully Treated with Pyridostigmine’ Neuromuscular Disorders Volume 32, Issue 2, February 2022, Pages 166-169

Published:2022-08 Issue:8 Volume:32 Page:e1
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Wyrebek Rita,Bartolomeo Mara Di,Brooks Sandra,Geller Thomas,Crenshaw Melissa,Iyadurai Stanley

Publisher

Elsevier BV

Subject

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

Cited by 2 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. Heterozygous c.175C>T variant in PURA gene causes severe developmental delay;Clinical Case Reports;2023-09

2. Neuromuscular and Neuromuscular Junction Manifestations of the PURA-NDD: A Systematic Review of the Reported Symptoms and Potential Treatment Options;International Journal of Molecular Sciences;2023-01-23

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