Abnormal protein translocation as the elusive cause of cystic fibrosis: an hypothesis

Author:

Herd J.K,Wagner D.H,LeClair I.O

Publisher

Elsevier BV

Subject

General Medicine

Reference101 articles.

1. Mendellian inheritance in man: Catalogues of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick,1978

2. Retraction: No evidence for more than one locus in cystic fibrosis;Danks;Am J Hum Genetics,1984

3. Incidence in Italy, genetic heterogeneity, and segregation analysis of cystic fibrosis;Romeo;Am J Hum Genetics,1985

4. A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7;Knowlton;Nature,1985

5. A closely linked genetic marker for cystic fibrosis;White;Nature,1985

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