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PHENOTYPIC AND GENETIC CHARACTERIZATION OF PATIENTS WITH FEATURES OF “NONCLASSIC” FORMS OF CYSTIC FIBROSIS
OBJECTIVE: To determine which features of incomplete or “nonclassic” forms of cystic fibrosis (CF) are associated with deleterious CF transmembrane conductance regulator gene (CFTR) mutations, and to explore other etiologies for features not associated with deleterious CFTR mutations. STUDY DESIGN:...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3380804/ https://ncbi.nlm.nih.gov/pubmed/15870673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpeds.2004.12.020 |
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