Hypokalemic Periodic Paralysis Type 2 Due to SCN4A Val1105Met Mutation: A Case Study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Aerospace Engineering
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3. Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study;Männikkö R;Lancet,2018
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5. Identification of a SCN4A mutation in a large Chinese family with atypical normokalemic periodic paralysis using whole-exome sequencing;Tan X;J Int Med Res,2020
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