No abstract available
MeSH terms
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Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
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Cystic Fibrosis* / complications
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Cystic Fibrosis* / genetics
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Cystic Fibrosis* / physiopathology
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Cystic Fibrosis* / therapy
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Early Diagnosis
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Exocrine Pancreatic Insufficiency* / genetics
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Exocrine Pancreatic Insufficiency* / therapy
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Female
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Humans
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Infant
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Italy
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Male
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Mutation*
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Pancreatic Function Tests / methods*
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Severity of Illness Index
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Time-to-Treatment / standards
Substances
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CFTR protein, human
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Cystic Fibrosis Transmembrane Conductance Regulator