Lack of Mutations of Preproparathyroid Hormone Gene in Three Kindreds with Familial Isolated Hypoparathyroidism.-Reference-Cited by-同舟云学术

Lack of Mutations of Preproparathyroid Hormone Gene in Three Kindreds with Familial Isolated Hypoparathyroidism.

Published:1997 Issue:1 Volume:44 Page:175-180
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

YAMAMOTO TOSHIKAZU¹,YOSHIMASA YASUNAO²,KOSHIYAMA HIROYUKI³,SUGIYAMA KYOKO¹,OKIGAKI MITSUHIKO¹,YAMADA TAKAYUKI¹,ISHII HITOSHI¹,YAGURA TOSHIHIRO¹,FUJIMOTO KAZUMITSU⁴,OHNISHI TOSHIAKI⁵,KOH TOSHIKIYO⁶,HINO MEGUMI⁷,KURAHACHI HIROYUKI⁸,YOSHIMASA TAKAAKI²,NAKAO KAZUWA²

Affiliation:

1. Departments of Endocrinology, Tenri Yorozu Hospital

2. Department of Medicine & Clinical Science, Kyoto University Graduate School of Medicine

3. Division of Endocrinology & Metabolism, Department of Internal Medicine, Hyogo Prefectural Amagasaki Hospital

4. Departments of Clinical Pathology, Tenri Yorozu Hospital

5. Ohnishi Naika Clinic

6. Division of Endocrinology, Department of Internal Medicine, Kyoto City Hospital

7. Departments of Nuclear Medicine, Kobe General Hospital

8. Departments of Endocrinology, Kobe General Hospital

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj1993/44/1/44_1_175/_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 novel mutation in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia in a family with two uncommon parathyroid hormone polymorphisms;Journal of Molecular Endocrinology;2003-10-01

2. Genetic Disorders of Calcium and Phosphorus Metabolism;Critical Reviews in Clinical Laboratory Sciences;2000-01