Associated Papers
Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences.
Ideozu JE et al.
Genome Medicine, 2024
38515211 (PubMed )
Supplement: 13073_2024_1316_MOESM1_ESM.xlsx › Table_S1A
Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
Löffler J et al.
European Journal of Human Genetics : Ejhg, 2001
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