Factor V Leiden 1601G > A (rs6025; p.Arg534Gln) mutation in pediatric cerebral palsy patients-Reference-Cited by-同舟云学术

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Factor V Leiden 1601G > A (rs6025; p.Arg534Gln) mutation in pediatric cerebral palsy patients

Published:2022-12 Issue: Volume:34 Page:201083
ISSN:2773-0441
Container-title:Human Gene
language:en
Short-container-title:Human Gene

Author:

Sreedevi N.,Swapna N.,Kovvali Srinivas,Maruthy Santosh,Kundapur Rajesh,Sylvester Charles

Funder

All India Institute of Speech and Hearing

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Factor V Leiden Mutation;Albagoush,2022

2. A genetic study of factor V Leiden (G1691A) mutation in young ischemic strokes with large vessel disease in a south Indian population;Anadure;J. Clin. Neurosci.,2017

3. Leiden V factor and spastic cerebral palsy in mexican children;Arenas-Sordo;Genet. Test. Mol. Biomark.,2012

4. Thrombosis;Ashorobi,2021

5. Factor V Leiden: is it the chief contributor to activated protein C resistance in Asian-Indian patients with deep vein thrombosis?;Biswas;Clin. Chim. Acta,2008

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