The mutation R672H in SCN4Agene exists in Chinese patients with hypokalaemic periodic paralysis

National Medical Journal of China

Volumn 86, Issue 11, 2006, Pages 724-727

  Ke, Qing ^a   Xu, Quan Gang ^b   Huang, De Hui ^b   Yuan, Hui Jun ^b   Zhao, Ya Li ^b   Wu, Wei Ping ^b  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b NONE

Author keywords

Calcium channels; Genes; Hypokalemic periodic paralysis; Mutation; Sodium channels

Indexed keywords

ACETAZOLAMIDE; GENE PRODUCT; POTASSIUM; PROTEIN SCN4A; UNCLASSIFIED DRUG; CALCIUM CHANNEL; SODIUM CHANNEL;

ADOLESCENT; ADULT; ARTICLE; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DRUG EFFICACY; EXON; FAMILY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; HYPOKALEMIC PERIODIC PARALYSIS; MALE; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; AGED; ASIAN; CASE REPORT; CHINA; ETHNOLOGY; GENETICS; MIDDLE AGED; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CALCIUM CHANNELS; CHINA; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; HYPOKALEMIC PERIODIC PARALYSIS; MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; POLYMERASE CHAIN REACTION; SODIUM CHANNELS;

EID: 33646045318     PISSN: 03762491     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

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