GATA3 abnormalities in six patients with HDR syndrome-Reference-Cited by-同舟云学术

GATA3 abnormalities in six patients with HDR syndrome

Published:2011 Issue:2 Volume:58 Page:117-121
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Fukami Maki¹,Muroya Koji²,Miyake Tetsuo¹³,Iso Manami¹,Kato Fumiko¹,Yokoi Hisashi⁴,Suzuki Yoshimi⁵,Tsubouchi Koji⁶,Nakagomi Yoshiko⁷,Kikuchi Nobuyuki⁸,Horikawa Reiko⁹,Ogata Tsutomu¹

Affiliation:

1. Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan

2. Department of Endocrinology and Metabolism, Kanagawa Children’s Medical Center, Yokohama, Japan

3. Department of Pediatrics, St. Marianna University Hospital, Kawasaki, Japan

4. Department of Internal Medicine, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan

5. Department of Pediatrics, Atsumi Hospital, Tawara, Japan

6. Department of Pediatrics, Mino Municipal Hospital, Mino, Japan

7. Department of Pediatrics, Yamanashi University Hospital, Yamanashi, Japan

8. Department of Pediatrics, Yokohama City University Hospital, Yokohama, Japan

9. Division of Endocrinology and Metabolism, National Medical Center for Children and Mothers, Tokyo, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.jstage.jst.go.jp/article/endocrj/58/2/58_K10E-234/_pdf

Reference10 articles.

1. Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia

2. GATA3 haplo-insufficiency causes human HDR syndrome

3. 3. Muroya K, Hasegawa T, Ito Y, Nagai T, Isotani H, Iwata Y, Yamamoto K, Fujimoto S, Seishu S, Fukushima Y, Hasegawa Y, Ogata T (2001) GATA3 abnormalities and the phenotypic spectrum of HDR syndrome. J Med Genet 38: 374-380.

4. The GATA-3 gene is expressed during human kidney embryogenesis

5. Embryonic expression of the human GATA-3 gene

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