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familial cylindromatosis
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Juan Jose Vilata Corell
Person without affiliation with CUNI
1 publication
Publication
publication
The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene
2016 |
Faculty of Medicine in Pilsen
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