A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations

Congenital heart diseases (CHDs) are still the leading cause of death in neonates. Anterior segment dysgenesis is a broad clinical phenotype that affects the normal development of the eye, leading in most of the cases to glaucoma which is still a major cause of blindness for children and adolescents...

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Detalhes bibliográficos
Publicado no:Front Cardiovasc Med
Main Authors: Khalil, Athar, Al-Haddad, Christiane, Hariri, Hadla, Shibbani, Kamel, Bitar, Fadi, Kurban, Mazen, Nemer, Georges, Arabi, Mariam
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2017
Assuntos:
Cardiovascular Medicine
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5611365/
https://ncbi.nlm.nih.gov/pubmed/28979898
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcvm.2017.00058
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