c.559 T>C as The Most Common Mutation of Factor XIII Deficiency in Iranian Patients is not Restricted to Southeast Iran

c.559 T>C as The Most Common Mutation of Factor XIII Deficiency in Iranian Patients is not Restricted to Southeast Iran

<p><strong>Background: </strong>Iran has a large group of patients with severe congenital factor XIII deficiency (FXIIID) and Trp187Arg mutation that is most disease causing mutation of FXIII in the world is only observed in southeast of Iran with 352 patients with FXIIID. 743 pati...

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Bibliographic Details
Main Authors: Akbar Dorgalaleh, Shadi Tabibian, Bijan Varmaghani, Gholam Hossein Tamaddon, Hasan Boustani
Format: Article
Language:English
Published: Shahid Beheshti University of Medical Sciences 2016-08-01
Series:Journal of Cellular and Molecular Anesthesia
Subjects:
Factor XIII deficiency, Trp187Arg mutation, Tehran Province
Online Access:http://journals.sbmu.ac.ir/jcma/article/view/13508

Internet

http://journals.sbmu.ac.ir/jcma/article/view/13508

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