Lack of association between urotensin-II (UTS2) gene polymorphisms (Thr21Met and Ser89Asn) and migraine

Migraine is a common neurovascular brain disorder with heterogeneous clinical presentation, including recurrent headache attacks. The pathophysiology of migraine is complex, and a number of genomic regions have been associated with the development of migraine. In this study, we analyzed the allele a...

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Vydáno v:Bosn J Basic Med Sci
Hlavní autoři: Ozan, Betül, Demiryürek, Seniz, Safdar, Muhammad, Inanc, Yusuf, Demiryürek, Abdullah Tuncay
Médium: Artigo
Jazyk:Inglês
Vydáno: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2017
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5581977/
https://ncbi.nlm.nih.gov/pubmed/28686849
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17305/bjbms.2017.2138
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