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
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Published in Pediatric pulmonology (01.06.2024)
Published in Pediatric pulmonology (01.06.2024)
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CFTR mutations and phenotypic correlations in people with cystic fibrosis: a retrospective study from a single centre in south India
Varkki, Sneha D., Aaron, Rekha, Chapla, Aaron, Danda, Sumita, Medhi, Priyanka, Jansi Rani, N., Paul, Grace R.
Published in The Lancet regional health. Southeast Asia (01.08.2024)
Published in The Lancet regional health. Southeast Asia (01.08.2024)
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CFTR mutations and phenotypic correlations in people with cystic fibrosis: a retrospective study from a single centre in south IndiaResearch in context
Sneha D. Varkki, Rekha Aaron, Aaron Chapla, Sumita Danda, Priyanka Medhi, N. Jansi Rani, Grace R. Paul
Published in The Lancet regional health. Southeast Asia (01.08.2024)
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Published in The Lancet regional health. Southeast Asia (01.08.2024)
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