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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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Detalles Bibliográficos
Autores principales:	Nimir, Mohammed, Abdelrahim, Mohanad, Abdelrahim, Mohamed, Abdalla, Mahil, Ahmed, Wala eldin, Abdullah, Muhanned, Hamid, Muzamil Mahdi Abdel
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	F1000 Research Limited 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814747/ https://www.ncbi.nlm.nih.gov/pubmed/29511529 http://dx.doi.org/10.12688/f1000research.10937.2

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