IndraLab

Statements


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sparser
"We describe a single family with affected members exhibiting either the FC or the MFT phenotypes associated with a mutation in the CYLD gene."

sparser
"MFT has been associated with mutations in the CYLD gene on a chromosome.[ xref ] Mutations in this gene have also been linked to familial cylindromatosis and Brooke–Spiegler syndrome, in which the patients develop trichoepitheliomas and cylindromas.[ xref ] CYLD gene has tumor suppressor properties and influences cell survival and proliferation."

sparser
"In this report, we describe three families with BSS, one with FC, and two with MFT phenotypes associated with novel and recurrent mutations in CYLD."