Periodic paralysis due to cumulative effects of rare variants in <scp> <i>SCN4A</i> </scp> with small functional alterations-Reference-Cited by-同舟云学术

Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterations

Published:2022-10-04 Issue:6 Volume:66 Page:757-761
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle and Nerve

Author:

Shibano Maki¹,Kubota Tomoya¹^ORCID,Kokubun Norito²,Miyaji Yosuke³,Kuriki Hiroko⁴,Ito Yuzuru⁵,Hamanoue Haruka⁴,Takahashi Masanori P.¹^ORCID

Affiliation:

1. Clinical Neurophysiology, Department of Clinical Laboratory and Biomedical Sciences, Division of Health Sciences Osaka University Graduate School of Medicine Suita Japan

2. Department of Neurology Dokkyo Medical University Shimotsuga Japan

3. Department of Neurology and Stroke Medicine Yokohama City University Graduate School of Medicine Yokohama Japan

4. Department of Clinical Genetics Yokohama City University Graduate School of Medicine Yokohama Japan

5. Department of Endocrinology and Metabolism Yokohama City University Medical Center Yokohama Japan

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Ministry of Health, Labour and Welfare

Mochida Memorial Foundation for Medical and Pharmaceutical Research

Takeda Science Foundation

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.27725

Reference21 articles.

1. Channelopathies of Skeletal Muscle Excitability

2. PATHOMECHANISMS IN CHANNELOPATHIES OF SKELETAL MUSCLE AND BRAIN

3. Defective slow inactivation of sodium channels contributes to familial periodic paralysis

4. Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

5. Gating pore current in an inherited ion channelopathy

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3. Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan;Frontiers in Neurology;2023-01-26