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Amedeo Smart

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Kumar M, Aaron R, Varkki SD, Danda S, et al. 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 Reunion, France. Pediatr Pulmonol 2024;59:1820-1825.
PMID: 38501349


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