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Autor:
Véronique Ladeveze, Hugo Talbot, Alain Kitzis, Ayman El-Seedy, Catherine Adolphe, Marie-Claude Pasquet, Caroline Norez, Raí«d Farhat
Publikováno v:
Cellular and molecular biology (Noisy-le-Grand, France). 63(11)
Cystic Fibrosis is the most common recessive autosomal rare disease found in Caucasian. It is caused by mutations on the Cystic Fibrosis Transmembrane Conductance Regulator gene (CFTR) that encodes for a protein located on the apical membrane of epit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26ac77068e715d11b546c4362d262c07
https://pubmed.ncbi.nlm.nih.gov/29208182
https://pubmed.ncbi.nlm.nih.gov/29208182
