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International Journal of Endocrinology
Volume 2014, Article ID 185974, 6 pages
http://dx.doi.org/10.1155/2014/185974
Research Article

Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency

1Division of Clinical Genetics, Department of Pediatrics, Children’s University Hospital Zagreb, Klaiceva 16, 10000 Zagreb, Croatia
2Steroid Disorder Program, Department of Pediatrics, Mount Sinai School of Medicine, New York, NY 10029, USA
3Tissue Typing Centre, University Hospital Centre Zagreb, 10000 Zagreb, Croatia
4Department of Laboratory Medicine, University Hospital Centre Zagreb, 10000 Zagreb, Croatia

Received 9 February 2014; Revised 1 May 2014; Accepted 5 May 2014; Published 2 June 2014

Academic Editor: Małgorzata Kotula-Balak

Copyright © 2014 Katja Dumic 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

Katja Dumic, Tony Yuen, Zorana Grubic, Vesna Kusec, Ingeborg Barisic, and Maria I. New, “Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11β-Hydroxylase Deficiency,” International Journal of Endocrinology, vol. 2014, Article ID 185974, 6 pages, 2014. https://doi.org/10.1155/2014/185974.