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Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseMolecular BiologyPathologyNeural Tube DefectsMolecular GeneticsC677t MutationFrench PatientsDisease Gene IdentificationMedicineNeurogenetics