TSHR mutations as a cause of congenital hypothyroidism in Japan: A population-based genetic epidemiology study

Journal of Clinical Endocrinology and Metabolism

Volumn 94, Issue 4, 2009, Pages 1317-1323

  Narumi, Satoshi ^a   Muroya, Koji ^b   Abe, Yoichiro ^a   Yasui, Masato ^a   Asakura, Yumi ^b   Adachi, Masanori ^b,c   Hasegawa, Tomonobu ^a  

^a KEIO UNIVERSITY   (Japan)

^b KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

^c Kanagawa Physicians Association   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

THYROTROPIN RECEPTOR;

ADOLESCENT; ADULT; ALLELE; ANIMAL CELL; ARTICLE; CHILD; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; GENE MUTATION; GENE SEQUENCE; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN SCREENING; NONHUMAN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PREVALENCE; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 65249173572     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2008-1767     Document Type: Article

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