In silico analysis of single nucleotide polymorphisms (SNPs) in human FOXC2 gene

Introduction: Lymphedema is an abnormal accumulation of interstitial fluid, due to inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. Methods: We identifie...

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Опубликовано в: :F1000Res
Главные авторы: Nimir, Mohammed, Abdelrahim, Mohanad, Abdelrahim, Mohamed, Abdalla, Mahil, Ahmed, Wala eldin, Abdullah, Muhanned, Hamid, Muzamil Mahdi Abdel
Формат: Artigo
Язык:Inglês
Опубликовано: F1000 Research Limited 2017
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Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5814747/
https://ncbi.nlm.nih.gov/pubmed/29511529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.10937.2
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