Gene Therapy of Cystic Fibrosis Lung Disease Using E1 Deleted Adenoviruses: A Phase I Trial. University of Michigan, Ann Arbor, Michigan and University of Pennsylvania, Philadelphia, Pennsylvania

James M. Wilson; John F. Engelhardt; Mariann Grossman; Richard H. Simon; Yiping Yang

Journal Article

Gene Therapy of Cystic Fibrosis Lung Disease Using E1 Deleted Adenoviruses: A Phase I Trial. University of Michigan, Ann Arbor, Michigan and University of Pennsylvania, Philadelphia, Pennsylvania

Wilson J
Engelhardt J
Grossman M
et al.

Human Gene Therapy (1994) 5(4) 501-519

DOI: 10.1089/hum.1994.5.4-501

N/ACitations

2Readers

Get full text

Abstract

I. Abstract Cystic fibrosis (CF) is an autosomal recessive disorder caused by defective ion transport across various epithelia. Multiple organ systems are affected in this disease; however, the pul...

Cite

CITATION STYLE

APA

Wilson, J. M., Engelhardt, J. F., Grossman, M., Simon, R. H., & Yang, Y. (1994). Gene Therapy of Cystic Fibrosis Lung Disease Using E1 Deleted Adenoviruses: A Phase I Trial. University of Michigan, Ann Arbor, Michigan and University of Pennsylvania, Philadelphia, Pennsylvania. Human Gene Therapy, 5(4), 501–519. https://doi.org/10.1089/hum.1994.5.4-501

Gene Therapy of Cystic Fibrosis Lung Disease Using E1 Deleted Adenoviruses: A Phase I Trial. University of Michigan, Ann Arbor, Michigan and University of Pennsylvania, Philadelphia, Pennsylvania

Abstract

Cite

Register to see more suggestions