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Case Reports in Genetics
Volume 2015, Article ID 301264, 5 pages
http://dx.doi.org/10.1155/2015/301264
Case Report

A Novel PHEX Mutation in Japanese Patients with X-Linked Hypophosphatemic Rickets

1Division of Endocrinology and Metabolism, Department of Internal Medicine, Niigata Rosai Hospital, Niigata 9428502, Japan
2Department of Clinical Laboratory, Niigata National Hospital, Niigata 9458585, Japan
3Department of Pharmacy, College of Pharmaceutical Sciences, Ritsumeikan University, Shiga 5258577, Japan
4Tokyo Women’s Medical University, Institute of Integrated Medical Sciences, Tokyo 1620054, Japan
5Department of Clinical Research, Saigata National Hospital, Niigata 9493193, Japan

Received 18 January 2015; Revised 28 February 2015; Accepted 5 March 2015

Academic Editor: Mohnish Suri

Copyright © 2015 Tetsuya Kawahara et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Tetsuya Kawahara, Hiromi Watanabe, Risa Omae, Toshiyuki Yamamoto, and Tetsuya Inazu, “A Novel PHEX Mutation in Japanese Patients with X-Linked Hypophosphatemic Rickets,” Case Reports in Genetics, vol. 2015, Article ID 301264, 5 pages, 2015. https://doi.org/10.1155/2015/301264.