Full Text
Full text is available in PDF
International Journal of Endocrinology and Metabolism
Research Institute for Endocrine Sciences
A Novel Mutation of SLC26A4 Gene In an Iranian Family with Pendred Syndrome
Author(s):
1Genetic Research Center, University of Social Walfare and Rehabilitation Sciences, Iran
2Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of Iowa, IA, USA
3Genetic Research Center, University of Social Walfare and Rehabilitation Sciences, hnajm@mavara.com, Iran
Article type:Research Article
Received:Jan 01, 2004
Accepted:Mar 01, 2005
How to Cite:K KahriziC NishimuraA NaghaviY RiazalhosseiniRJH SmithH Najmabadiet al.A Novel Mutation of SLC26A4 Gene In an Iranian Family with Pendred Syndrome.Int J Endocrinol Metab.3(2):104-108.
Abstract
Copyright
© 0, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
comments
Leave a comment here
Comments
Number of Comments:0Purchasing Reprints
- Copyright Clearance Center (CCC) handles bulk orders for article reprints for Brieflands. To place an order for reprints, please click here ( https://www.copyright.com/landing/reprintsinquiryform/ ). Clicking this link will bring you to a CCC request form where you can provide the details of your order. Once complete, please click the ‘Submit Request’ button and CCC’s Reprints Services team will generate a quote for your review.
Search Relations
Author(s):
Related Articles