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International Journal of Endocrinology
Volume 2015 (2015), Article ID 595164, 5 pages
http://dx.doi.org/10.1155/2015/595164
Research Article

A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy

1Department of Pediatrics, Aseer Central Hospital, Abha 62523, Saudi Arabia
2Department of Child Health, College of Medicine, King Khalid University, Abha 61421, Saudi Arabia
3Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia

Received 11 May 2015; Revised 28 June 2015; Accepted 29 June 2015

Academic Editor: Franco Veglio

Copyright © 2015 Mohammad A. Alqahtani 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

Mohammad A. Alqahtani, Ayed A. Shati, Minjing Zou, et al., “A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy,” International Journal of Endocrinology, vol. 2015, Article ID 595164, 5 pages, 2015. doi:10.1155/2015/595164