Cargando…

Methylenetetrahydrofolate reductase C677T variant in Indian children with craniosynostosis: Its role in the pathogenesis, risk of craniosynostosis

BACKGROUND: 677C to T allele in the 5, 10-methylenetetrahydrofolate reductase (MTHFR) gene has been implicated in the etiology of various syndromes and nonsyndromic diseases but till date no direct studies have been reported with craniosynostosis. OBJECTIVES: The aim was to study the family-based as...

Descripción completa

Detalles Bibliográficos
Autores principales: Pandey, Rajeev Kumar, Ali, Abid, Singh, Amit, Gayan, Sukanya, Bajpai, Minu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228567/
https://www.ncbi.nlm.nih.gov/pubmed/25400344
http://dx.doi.org/10.4103/0971-6866.142882

Ejemplares similares