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

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📜 SIMILAR VOLUMES

192 Late diagnosed cystic fibrosis (CF)

✍ J. Miller; S. Doe; A. Gascoigne; S. Bourke 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 43 KB

53 Lung function, weight, and sweat chlo

✍ Plant, B.J.; Konstan, M.; Aherns, R.; Rodriguez, S.; Munck, A.; Elborn, J.S.; Jo 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 73 KB

PHENOTYPIC VARIABILITY IN A FAMILY WITH

✍ V. Lucidi; F. Alghisi; A. Angioni; A.C. Tomaiuolo; M.R. D'Apice; S. Gambardella; 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 54 KB

WS7.6 Effect of ivacaftor on lung functi

✍ J.C. Davies; H. Sheridan; P.-S. Lee; T. Song; A. Stone; F. Ratjen 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 60 KB

Mild cystic fibrosis and normal or borde

✍ A. Augarten; Y. Yahav; A. Szeinberg; S. Noiman; E. Gazit; B-S. Kerem; Y. Rivlin; 📂 Article 📅 1993 🏛 The Lancet 🌐 English ⚖ 333 KB

Malignant mutation in the lamin A/C gene

✍ Loizos Antoniades; Christos Eftychiou; Theodoros Kyriakides; Kyproula Christodou 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 303 KB