Missense mutation R1066C in the second transmembrane domain...

Human Mutation 1997 Vol. 10; Iss. 5

Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: Study of 19 heterozygous and 2 homozygous patients

T Casals, P Pacheco, C Barreto, J Giménez, MD Ramos, S Pereira, JA Pinheiro, N Cobos, A Curvelo, C Vázquez, H Rocha, JL Séculi, E Pérez, J Dapena, E Carrilho, A Duarte, AM Palacio, V Nunes, J Lavinha,
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Volume:
10
Year:
1997
Language:
english
Pages:
6
DOI:
10.1002/(sici)1098-1004(1997)10:53.0.co;2-c
File:
PDF, 157 KB
english, 1997
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