Haplotype analysis reveals founder effects of thyroglobulin gene mutations C1058R and C1977S in Japan

Journal of Clinical Endocrinology and Metabolism

Volumn 91, Issue 8, 2006, Pages 3100-3104

  Hishinuma, Akira ^a   Fukata, Shuji ^b   Nishiyama, Soroku ^c   Nishi, Yoshikazu ^d   Oh Ishi, Masamichi ^e   Murata, Yoshiharu ^f   Ohyama, Yoshihide ^g   Matsuura, Nobuo ^e   Kasai, Kikuo ^a   Harada, Shohei ^h   Kitanaka, Sachiko ⁱ   Takamatsu, Junta ^j   Kiwaki, Kohji ^c   Ohye, Hidemi ^b   Uruno, Takashi ^b   Tomoda, Chisato ^b   Tajima, Toshihiro ^k   Kuma, Kanji ^b   Miyauchi, Akira ^b   Ieiri, Tamio ^a  

^a DOKKYO MEDICAL UNIVERSITY   (Japan)

^b KUMA HOSPITAL   (Japan)

^c KUMAMOTO UNIVERSITY   (Japan)

^d ATOMIC BOMB SURVIVORS HOSPITAL   (Japan)

^e KITASATO UNIVERSITY   (Japan)

^f NAGOYA UNIVERSITY   (Japan)

^g Ohyama Clinic   (Japan)

^h NATIONAL CENTER FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

ⁱ UNIVERSITY OF TOKYO   (Japan)

^j Takamatsu Thyroid Clinic   (Japan)

^k HOKKAIDO UNIVERSITY   (Japan)

more..

Author keywords

[No Author keywords available]

Indexed keywords

LIOTRIX; THYROGLOBULIN; THYROID HORMONE;

ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DEMOGRAPHY; FOUNDER EFFECT; GENE IDENTIFICATION; GENE MUTATION; GOITER; HAPLOTYPE; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; JAPAN; MAJOR CLINICAL STUDY; PREVALENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 33747686032     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2005-2702     Document Type: Article

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