A Mutation in Tpst2 Encoding Tyrosylprotein Sulfotransferase Causes Dwarfism Associated with Hypothyroidism-Reference-Cited by-同舟云学术

A Mutation in Tpst2 Encoding Tyrosylprotein Sulfotransferase Causes Dwarfism Associated with Hypothyroidism

Published:2007-07-01 Issue:7 Volume:21 Page:1713-1721
ISSN:0888-8809
Container-title:Molecular Endocrinology
language:en
Short-container-title:

Author:

Sasaki Nobuya¹,Hosoda Yayoi¹,Nagata Aogu¹,Ding Ming²,Cheng Ji-Ming²,Miyamoto Tomomi²,Okano Shinya¹,Asano Atsushi¹,Miyoshi Ichiro²,Agui Takashi¹

Affiliation:

1. Laboratory of Experimental Animal Science (N.S., Y.H., A.N., S.O., A.A., T.A.), Graduate School of Veterinary Medicine, Hokkaido University, Kita-ku, Sapporo 060-0818, Japan

2. Center for Experimental Animal Science (M.D., J.-M.C., T.M., I.M.), Nagoya City University Medical School, Mizuho-ku, Nagoya 467-8601, Japan

Publisher

The Endocrine Society

Subject

Endocrinology,Molecular Biology,General Medicine

Link

http://academic.oup.com/mend/article-pdf/21/7/1713/8961950/mend1713.pdf

Reference39 articles.

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2. Resistance to TSH.;Refetoff;J Endocrinol Invest,2003

3. Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2–1 haploinsufficiency.;Lafferty;J Clin Invest,2002

4. Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.;Pohlenz;J Clin Invest,2002

5. Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia.;Clifton-Bligh;Nat Genet,1998

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