Missense Mutation R1066C in the Second Transmembrane Domain of Cftr Causes a Severe Cystic Fibrosis Phenotype: Study of 19 Heterozygous and 2 Homozygous Patients

AuthID
P-001-CGB
20
Author(s)
Casals, T
·
Pacheco, P
·
Gimenez, J
·
Ramos, MD
·
Pinheiro, JA
·
Cobos, N
·
Curvelo, A
·
Vazquez, C
·
Rocha, H
·
Perez, E
·
Dapena, J
·
Carrilho, E
·
Duarte, A
·
Palacio, AM
·
Nunes, V
·
Lavinha, J
·
Estivill, X
Tipo de Documento
Article
Year published
1997
Publicado
in HUMAN MUTATION, ISSN: 1059-7794
Volume: 10, Número: 5, Páginas: 387-392 (6)
Indexing
Publication Identifiers
Pubmed: 9375855
SCOPUS: 2-s2.0-16944365624
Wos: WOS:A1997YC78600009
Source Identifiers
ISSN: 1059-7794
Export Publication Metadata
Citações
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Journal Factors
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