Mutations in Exon 7 of the GTP-Binding Protein Gs.ALPHA. Were Not a Common Cause of Pseudohypoparathyroidism with Albright's Hereditary Osteodystrophy in Japanese.-Reference-Cited by-同舟云学术

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Mutations in Exon 7 of the GTP-Binding Protein Gs.ALPHA. Were Not a Common Cause of Pseudohypoparathyroidism with Albright's Hereditary Osteodystrophy in Japanese.

Published:1997 Issue:4 Volume:44 Page:621-625
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

TAKEDA KYOKO¹,YOKOYAMA MINAO²,HASHIMOTO KOZO²,HIROMATSU YUJI³,YAMANAKA HIDEKATA⁴,SHIMIZU TAEKO⁵,SASAKI MASAHIDE¹

Affiliation:

1. Department of Clinical Laboratory Medicine, Kochi Medical School

2. Second Department of Internal Medicine, Kochi Medical School

3. Fourth Department of Internal Medicine, Kurume Medical School

4. Miyazaki Prefectural Hospital

5. Toranomon Hospital

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj1993/44/4/44_4_621/_pdf

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Pseudohypoparathyroidism Type Ia Patient with Normocalcemia;Endocrine Journal;2008

2. Pseudohypoparathyroidism;The Parathyroids;2001

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