Identification of 99% of CFTR gene mutations in Bulgarian ‐, Bulgarian Turk‐, and Roma cystic fibrosis patients
ConclusionThis collaborative study improves genetic counselling in BG, facilitates introduction of multitier CF neonatal screening and fosters public health measures for improvement of care in the Roma CF population.
Source: Molecular Genetics & Genomic Medicine - Category: Genetics & Stem Cells Authors: Guergana Petrova,
Nadezhda Yaneva,
Jana Hrbkov á,
Malgorzata Libik,
Alexey Savov,
Milan Macek Tags: ORIGINAL ARTICLE Source Type: research