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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Detalhes bibliográficos
Publicado no:F1000Res
Main Authors: Nimir, Mohammed, Abdelrahim, Mohanad, Abdelrahim, Mohamed, Abdalla, Mahil, Ahmed, Wala eldin, Abdullah, Muhanned, Hamid, Muzamil Mahdi Abdel
Formato: Artigo
Idioma:Inglês
Publicado em: F1000 Research Limited 2017
Assuntos:
Research Article
Acesso em linha: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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