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BioMed Research International
Volume 2015 (2015), Article ID 517815, 8 pages
http://dx.doi.org/10.1155/2015/517815
Research Article

A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis

1Molecular Genetics and Enzymology Department, Human Genetics & Genome Research Division, National Research Centre, 33 El Bohouth Street (Former El Tahrir Street), P.O. Box 12622, Dokki, Giza, Egypt
2Clinical Genetics Department, Human Genetics & Genome Research Division, National Research Centre, Egypt
3Department of Medicine, Faculty of Medicine, Cairo University, Egypt
4Department of Orodental Genetics, Medical Research Division, National Research Centre, Egypt

Received 4 January 2015; Revised 13 March 2015; Accepted 29 March 2015

Academic Editor: Jozef Zustin

Copyright © 2015 Alaaeldin Fayez 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

Alaaeldin Fayez, Mona Aglan, Nora Esmaiel, Taher El Zanaty, Mohamed Abdel Kader, and Mona El Ruby, “A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis,” BioMed Research International, vol. 2015, Article ID 517815, 8 pages, 2015. doi:10.1155/2015/517815