Screening for C677T and A1298C MTHFR polymorphisms in patients with epilepsy and risk of hyperhomocysteinemia.

Caccamo, D; Condello, S; Gorgone, G; Crisafulli, G; Belcastro, V; Gennaro, S; Striano, P; Pisani, F; Ientile, R

Caccamo, D; Condello, S; Gorgone, G; Crisafulli, G; Belcastro, V; Gennaro, S; Striano, P; Pisani, F; Ientile, R.

Affiliation

Caccamo D; Department of Biochemical, Physiological and Nutritional Sciences, University of Messina, Via Consolare Valeria, Policlinico Universitario, 98125 Messina, Italy. dcaccamo@unime.it

Neuromolecular Med ; 6(2-3): 117-26, 2004.

Article in En | MEDLINE | ID: mdl-15970629

Subject(s)

Epilepsy/genetics; Hyperhomocysteinemia/genetics; Methylenetetrahydrofolate Reductase (NADPH2)/genetics; Polymorphism, Single Nucleotide; Adolescent; Adult; Aged; Amino Acid Substitution; Base Sequence; DNA Primers; Female; Genotype; Humans; Hyperhomocysteinemia/complications; Male; Middle Aged; Reference Values; Risk Factors

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Collection: 01-internacional Database: MEDLINE Main subject: Hyperhomocysteinemia / Polymorphism, Single Nucleotide / Methylenetetrahydrofolate Reductase (NADPH2) / Epilepsy Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies / Screening_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Neuromolecular Med Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA Year: 2004 Type: Article Affiliation country: Italy

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