A rare variant c.1802T>C (p. Ile601Thr) associated with severe phenotype among people with cystic fibrosis from south India, and potential genetic admixture in Réunion, France
PEDIATRIC PULMONOLOGY（2024）
Key words
cystic fibrosis,rare variant c.1802T > C (p. Ile601Thr),Reunion, France,South India
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