A novelGJA1mutation in oculodentodigital dysplasia with extensive loss of enamel-Reference-Cited by-同舟云学术

A novelGJA1mutation in oculodentodigital dysplasia with extensive loss of enamel

Published:2017-04-03 Issue:6 Volume:23 Page:795-800
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:Oral Dis

Author:

Porntaveetus T¹²,Srichomthong C³⁴,Ohazama A⁵,Suphapeetiporn K³⁴^ORCID,Shotelersuk V³⁴

Affiliation:

1. Department of Physiology; Faculty of Dentistry; Chulalongkorn University; Bangkok Thailand

2. STAR on Craniofacial and Skeletal Disorders; Chulalongkorn University; Bangkok Thailand

3. Department of Pediatrics; Center of Excellence for Medical Genetics; Faculty of Medicine; Chulalongkorn University; Bangkok Thailand

4. Excellence Center for Medical Genetics; King Chulalongkorn Memorial Hospital; Bangkok Thailand

5. Division of Oral Anatomy; Niigata University; Niigata Japan

Funder

Thailand Research Fund

Ratchadapisek Sompoch Endowment Fund

Chulalongkorn University

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/odi.12663/fullpdf

Reference28 articles.

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4. Combinatorial expression patterns of the connexins 26, 32, and 43 during development, homeostasis, and regeneration of rat teeth;Fried;Int J Dev Biol,1996

5. Oculodentodigital dysplasia: new ocular findings and a novel connexin 43 mutation;Gabriel;Arch Ophthalmol,2011

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