J. L. Seculi
AuthID: R-00G-C9Z
1
TITLE: Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: Study of 19 heterozygous and 2 homozygous patients Full Text
AUTHORS: Casals, T; Pacheco, P; Barreto, C; Gimenez, J; Ramos, MD; Pereira, S; Pinheiro, JA; Cobos, N; Curvelo, A; Vazquez, C; Rocha, H; Seculi, JL; Perez, E; Dapena, J; Carrilho, E; Duarte, A; Palacio, AM; Nunes, V; Lavinha, J; Estivill, X;
PUBLISHED: 1997, SOURCE: HUMAN MUTATION, VOLUME: 10, ISSUE: 5
AUTHORS: Casals, T; Pacheco, P; Barreto, C; Gimenez, J; Ramos, MD; Pereira, S; Pinheiro, JA; Cobos, N; Curvelo, A; Vazquez, C; Rocha, H; Seculi, JL; Perez, E; Dapena, J; Carrilho, E; Duarte, A; Palacio, AM; Nunes, V; Lavinha, J; Estivill, X;
PUBLISHED: 1997, SOURCE: HUMAN MUTATION, VOLUME: 10, ISSUE: 5
