학술논문
Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: Study of 19 heterozygous and 2 homozygous patients.
Document Type
Article
Author
Source
Human Mutation; 1997, Vol. 10 Issue 5, p387-392, 6p
Subject
Language
ISSN
10597794