A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides [1]

W. E. Highsmith, K. J. Friedman, L. H. Burch, A. Spock, L. M. Silverman, R. C. Boucher, Michael R. Knowles

Research output: Contribution to journalLetter

14 Scopus citations
Original languageEnglish (US)
Pages (from-to)88-90
Number of pages3
JournalClinical Genetics
Volume68
Issue number1
DOIs
StatePublished - Jul 2005

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Highsmith, W. E., Friedman, K. J., Burch, L. H., Spock, A., Silverman, L. M., Boucher, R. C., & Knowles, M. R. (2005). A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides [1]. Clinical Genetics, 68(1), 88-90. https://doi.org/10.1111/j.1399-0004.2005.00459.x