R450H TSH receptor mutation in congenital hypothyroidism in Taiwanese children

Clinica Chimica Acta

Volumn 413, Issue 11-12, 2012, Pages 1004-1007

  Chang, Wei Chiao ^a,b   Liao, Cheng Yu ^b   Chen, Wei Chiao ^a   Fan, Yung Ching ^a   Chiu, Siou Jin ^a   Kuo, Ho Chang ^d,e   Woon, Peng Yeong ^c   Chao, Mei Chyn ^a,b  

^a KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

^b KAOHSIUNG MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^c TZU CHI UNIVERSITY   (Taiwan)

^d CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^e CHANG GUNG UNIVERSITY COLLEGE OF MEDICINE   (Taiwan)

Author keywords

Congenital hypothyroidism; Genetic mutation; TSH receptor

Indexed keywords

THYROTROPIN RECEPTOR;

ALLELE; ARTICLE; CASE CONTROL STUDY; CHILD; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DEVELOPMENTAL GENE; ETHNIC GROUP; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; HEALTH STATUS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; TAIWANESE; THYROTROPIN BLOOD LEVEL; TSHR GENE;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CONGENITAL HYPOTHYROIDISM; FEMALE; GENE FREQUENCY; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; RECEPTORS, THYROTROPIN; REFERENCE VALUES; TAIWAN; THYROTROPIN; YOUNG ADULT;

EID: 84862827106     PISSN: 00098981     EISSN: 18733492     Source Type: Journal    
DOI: 10.1016/j.cca.2012.02.027     Document Type: Article

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