U. Fanhoe
AuthID: R-00G-P3W
1
TITLE: Molecular characterization of five patients with homocystinuria due to severe methylenetetrahydrofolate reductase deficiency Full Text
AUTHORS: Urreizti, R; Moya Garcia, AA; Pino Angeles, A; Cozar, M; Langkilde, A; Fanhoe, U; Esteves, C; Arribas, J; Vilaseca, MA; Perez Duenas, B; Pineda, M; Gonzalez, V; Artuch, R; Baldellou, A; Vilarinho, L; Fowler, B; Ribes, A; Sanchez Jimenez, F; Grinberg, D; Balcells, S;
PUBLISHED: 2010, SOURCE: CLINICAL GENETICS, VOLUME: 78, ISSUE: 5
AUTHORS: Urreizti, R; Moya Garcia, AA; Pino Angeles, A; Cozar, M; Langkilde, A; Fanhoe, U; Esteves, C; Arribas, J; Vilaseca, MA; Perez Duenas, B; Pineda, M; Gonzalez, V; Artuch, R; Baldellou, A; Vilarinho, L; Fowler, B; Ribes, A; Sanchez Jimenez, F; Grinberg, D; Balcells, S;
PUBLISHED: 2010, SOURCE: CLINICAL GENETICS, VOLUME: 78, ISSUE: 5
