The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America (vol 51, pg 305, 2007)

Univ Barcelona, Fac Biol, Dept Genet, E-08028 Barcelona, SpainUniv Nacl Cordoba, Ctr Estudio Metab Congenitas, RA-5000 Cordoba, ArgentinaPontificia Univ Javeriana, Inst Genet Humana, Bogota, ColombiaUniv Antioquia, Fac Med, Dept Fisiol & Bioquim, Medellin, ColombiaFdn Estudio Enfermedades Neurometab, Buenos Aires, DF, ArgentinaInst Genet Med Jacinto Magalhaes, Oporto, PortugalUniversidade Federal de São Paulo, EPM, UNIFESP, Dept Pediat, São Paulo, BrazilHosp Ramon & Cajal, Serv Pediat, Unidad Enfermedades Metab, E-28034 Madrid, SpainHosp Univ Materno Infantil, Unidad Gastroenterol & Nutr, Las Palmas Gran Canaria, SpainHosp Infantil La Fe, Unidad Nutr & Metab, Valencia, SpainHosp Clin Univ Santiago, Dept Pediat, Santiago de Compostela, SpainCorp Sanitaria Clin, Inst Bioquim Clin, Barcelona, SpainHosp St Joan Deu, Serv Bioquim, Barcelona, SpainUniversidade Federal de São Paulo, EPM, UNIFESP, Dept Pediat, São Paulo, BrazilWeb of Scienc