The α1S subunit of the L-type calcium channel is not a predisposition gene for thyrotoxic periodic paralysis

Clinical Endocrinology

Volumn 66, Issue 2, 2007, Pages 229-234

  Tang, Nelson L S ^a,b   Chow, C C ^a   Ko, Gary T C ^c   Tai, Morris H L ^a   Kwok, Rachel ^a   Yao, X Q ^a   Cockram, Clive S ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b Prince of Wales Hospital   (Hong Kong)

^c ALICE HO MIU LING NETHERSOLE HOSPITAL   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL L TYPE;

ADULT; ARTICLE; CHINESE; CONTROLLED STUDY; GENE; GENE DELETION; GENE INSERTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; THYROID DISEASE; THYROTOXIC PERIODIC PARALYSIS;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CALCIUM CHANNELS; CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; HYPOKALEMIC PERIODIC PARALYSIS; MALE; MIDDLE AGED; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33846256189     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2006.02713.x     Document Type: Article

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