Prevalence and Novel Mutations of Lysosomal Storage Disorders in United Arab Emirates-Reference-Cited by-同舟云学术

Prevalence and Novel Mutations of Lysosomal Storage Disorders in United Arab Emirates

Published:2012 Issue: Volume: Page:1-9
ISSN:2192-8304
Container-title:JIMD Reports
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Author:

Al-Jasmi Fatma A.,Tawfig Nafisa,Berniah Ans,Ali Bassam R.,Taleb Mahmoud,Hertecant Jozef L.,Bastaki Fatma,Souid Abdul-Kader

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/8904_2012_182

Reference24 articles.

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2. Al-Gazali LI, Bener A et al (1997) Consanguineous marriages in the United Arab Emirates. J Biosoc Sci 29(4):491–497

3. Ali BR, Hertecant JL et al (2011) New and known mutations associated with inborn errors of metabolism in a heterogeneous Middle Eastern population. Saudi Med J 32(4):353–359

4. Al-Jasmi F (2012) A novel mutation in an atypical presentation of the rare infantile Farber disease. Brain Dev 34(6):533–535

5. Bach G, Moskowitz SM et al (1993) Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic area. Am J Hum Genet 53(2):330–338

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