Familial hyperkalemic periodic paralysis caused by ade novomutation in the sodium channel geneSCN4A
Author:
Affiliation:
1. Department of Pediatrics, Konyang University College of Medicine, Daejeon, Korea.
Publisher
Korean Pediatric Society
Subject
Pediatrics,Pediatrics, Perinatology and Child Health
Link
http://kjp.or.kr/upload/pdf/kjped-54-470.pdf
Reference15 articles.
1. Hyperkalemic periodic paralysis: Rapid molecular diagnosis and relationship of genotype to phenotype in 12 families
2. Genotype-Phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis
3. Reliability and validity of the Medical Research Council (MRC) scale and a modified scale for testing muscle strength in patients with radial palsy
4. An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel geneSCN4A
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3. Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review;Case Reports in Genetics;2020-10-16
4. Treatment and Management of Neuromuscular Channelopathies;Current Treatment Options in Neurology;2014-08-15
5. Molecular cloning of ion channels in Felis catus that are related to periodic paralyses in man: a contribution to the understanding of the genetic susceptibility to feline neck ventroflexion and paralysis;Biology Open;2014-07-25
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