Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan | Zendy

Akira Hishinuma | Zendy; Shuji Fukata | Zendy; Soroku Nishiyama | Zendy; Yoshikazu Nishi | Zendy; Masamichi Ohishi | Zendy; Yoshiharu Murata | Zendy; Yoshihide Ohyama | Zendy; Nobuo Matsuura | Zendy; Kikuo Kasai | Zendy; Shohei Harada | Zendy; Sachiko Kitanaka | Zendy; Junta Takamatsu | Zendy; Kohji Kiwaki | Zendy; Hidemi Ohye | Zendy; Takashi Uruno | Zendy; Chisato Tomoda | Zendy; Toshihiro Tajima | Zendy; Kanji Kuma | Zendy; Akira Miyauchi | Zendy; Tamio Ieiri | Zendy

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Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan

Author(s) -

Akira Hishinuma,

Shuji Fukata,

Soroku Nishiyama,

Yoshikazu Nishi,

Masamichi Ohishi,

Yoshiharu Murata,

Yoshihide Ohyama,

Nobuo Matsuura,

Kikuo Kasai,

Shohei Harada,

Sachiko Kitanaka,

Junta Takamatsu,

Kohji Kiwaki,

Hidemi Ohye,

Takashi Uruno,

Chisato Tomoda,

Toshihiro Tajima,

Kanji Kuma,

Akira Miyauchi,

Tamio Ieiri

Publication year - 2006

Publication title -

the journal of clinical endocrinology and metabolism

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.206

H-Index - 353

eISSN - 1945-7197

pISSN - 0021-972X

DOI - 10.1210/jc.2005-2702

Subject(s) - thyroglobulin , endocrinology , medicine , context (archaeology) , euthyroid , haplotype , mutation , congenital hypothyroidism , genetics , biology , gene , thyroid , genotype , paleontology

Thyroglobulin (Tg) mutations were previously believed to be rare, resulting in congenital goitrous hypothyroidism. However, an increasing number of patients with Tg mutations, who are euthyroid to mildly hypothyroid, have been identified in Japan.

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