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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

Crossref DOI link: https://doi.org/10.1186/s12863-016-0346-9

Published Online: 2016-02-09

Published Print: 2016-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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