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
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| Description | scientific article published on 9 February 2016 |
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author: Tomas Vanecek Dmitry Kazakov |
| Publication date | February 9, 2016 |
| Language | English |
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