Study of C677T Methylene Tetrahydrofolate Reductase Gene Polymorphism as a Risk Factor for Neural Tube Defects.

Goyal, Anjalika; Kumawat, Manjulata; Vashisth, Minakshi; Gill, Paramjit Singh; Sing, Ishwar; Dhaulakhandi, Dhara B

Goyal, Anjalika; Kumawat, Manjulata; Vashisth, Minakshi; Gill, Paramjit Singh; Sing, Ishwar; Dhaulakhandi, Dhara B.

Afiliación

Goyal A; Department of Biochemistry, PGIMS, Pandit Bhagwat Dayal Sharma University of Health Sciences, Rohtak, Haryana, India.
Kumawat M; Department of Biochemistry, PGIMS, Pandit Bhagwat Dayal Sharma University of Health Sciences, Rohtak, Haryana, India.
Vashisth M; Department of Genetics, Maharshi Dayanand University, Rohtak, Haryana, India.
Gill PS; Department of Microbiology, Maharshi Dayanand University, Rohtak, Haryana, India.
Sing I; Department of Neurosurgery, PGIMS, Pandit Bhagwat Dayal Sharma University of Health Sciences, Rohtak, Haryana, India.
Dhaulakhandi DB; Department of Biotechnology and Molecular Medicine, PGIMS, Pandit Bhagwat Dayal Sharma University of Health Sciences, Rohtak, Haryana, India.

Asian J Neurosurg ; 16(3): 554-561, 2021.

Article en En | MEDLINE | ID: mdl-34660368

Palabras clave

Allele; association; methylene tetrahydrofolate reductase; neural tube defect; polymorphism

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Idioma: En Revista: Asian J Neurosurg Año: 2021 Tipo del documento: Article País de afiliación: India Pais de publicación: India

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