Intervention Protocol

Mutation-specific therapies that potentiate cystic fibrosis transmembrane conductance regulator (CFTR) function in cystic fibrosis

  1. Ian P Sinha1,*,
  2. Kevin W Southern1,
  3. Kerry Dwan1,
  4. Carlos Echevarria2,
  5. Michael Schechter3

Editorial Group: Cochrane Cystic Fibrosis and Genetic Disorders Group

Published Online: 16 MAY 2012

DOI: 10.1002/14651858.CD009841

Database Title

Additional Information

How to Cite

Sinha IP, Southern KW, Dwan K, Echevarria C, Schechter M. Mutation-specific therapies that potentiate cystic fibrosis transmembrane conductance regulator (CFTR) function in cystic fibrosis (Protocol). Cochrane Database of Systematic Reviews 2012, Issue 5. Art. No.: CD009841. DOI: 10.1002/14651858.CD009841.

Author Information

  1. 1

    University of Liverpool, Institute of Child Health, Liverpool, Merseyside, UK

  2. 2

    University Hospital of North Tees, Stockton, UK

  3. 3

    Emory University School of Medicine, Department of Paediatrics, Atlanta, Georgia, USA

*Ian P Sinha, Institute of Child Health, University of Liverpool, Alder Hey Children's Foundation Trust, Eaton Road, Liverpool, Merseyside, L12 2AP, UK. iansinha@liverpool.ac.uk.

Publication History

  1. Publication Status: New
  2. Published Online: 16 MAY 2012

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