CYTOMORPHOLOGY OF SKIN ADNEXAL TUMORS: A TALE OF TWO SCALP SWELLINGS





TINF2 Gene Mutation in a Patient with Pulmonary Fibrosis

Pulmonary fibrosis is a frequent manifestation of telomere syndromes.Telomere gene mutations are found in up to 25% and 3% of patients with familial disease and sporadic disease, respectively.The telomere gene TINF2 encodes an eponymous protein that is part of the shelterin complex, a complex involved in telomere protection and maintenance.A TINF2

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