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Hiperhomocistinemia y polimorfismo 677C → T de la 5,10-metilenotetrahidrofolato reductasa en hijos de pacientes con enfermedad coronaria prematura
Hyperhomocystinemia and 677C → T methylenetetrahydrofolate reductase polymorphism as a cardiovascular risk factor in childhood
C. Mainou Cida,
Corresponding author
mainou@medicina.ub.es

Correspondencia: Servicio de Pediatría. Hospital Sant Joan de Déu. P.° Sant Joan de Déu, 2. 08950 Esplugues. Barcelona
, N. García Giraltb, M.aA. Vilaseca Buscàc, I. Ferrer Codinac, José F. Meco Lópezd, A. Mainou Pintóa, X. Pintó Salad, D. Grinberg Vaismanb, S. Balcells Comasb
a Servicio de Pediatría. Hospital Universitario Sant Joan de Déu. Barcelona.
b Departamento de Genética. Facultad de Biología. Universidad de Barcelona.
c Servicio de Bioquímica. Hospital Universitario Sant Joan de Déu. Barcelona.
d Unidad de Aterosclerosis. CSUB.
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ISSN: 16954033
Original language: Spanish
DOI:10.1016/S1695-4033(02)77836-3
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