id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_nnbji256k5bqldsyuv4upr6iwu	Miesha Merati	Aggressive CD8+ epidermotropic cutaneous T-cell lymphoma associated with homozygous mutation in SAMHD1	2015.0	3	.pdf	application/pdf	1693	226	38	Key words: cutaneous T-cell lymphoma; SAM domain and HD domainecontaining protein 1. Mutations in the SAMHD1 (SAM domain and epidermotropic cutaneous T-cell lymphoma (CTCL). mutation c.1411-2A [ G in the SAMHD1 gene Dermatology, Case Western Reserve University School of dicine, UH Seidman Cancer Center, University Hospitals Case Skin biopsy from the abdomen showed significant mailto:Meg.Gerstenblith@uhhospitals.org mailto:Meg.Gerstenblith@uhhospitals.org Genomic instability caused by SAMHD1 mutations may lead to increased mutagenesis and cancer more aggressive clinical course.10 Our patient's CTCL with homozygous mutations of SAMHD1 could Study concept and design: Drs Merati, Buethe, Cooper, Merati, Buethe, Cooper, Honda, Wang, Gerstenblith Drafting of the manuscript: Drs Merati, Buethe, Cooper, intellectual content: Drs Merati, Buethe, Cooper, Honda, in SAMHD1 gene causes cerebral vasculopathy and early onset Syndrome Caused by the Arg164X Mutation in SAMHD1 Are Aggressive CD8+ epidermotropic cutaneous T-cell lymphoma associated with homozygous mutation in SAMHD1 Aggressive CD8+ epidermotropic cutaneous T-cell lymphoma associated with homozygous mutation in SAMHD1	./cache/work_nnbji256k5bqldsyuv4upr6iwu.pdf	./txt/work_nnbji256k5bqldsyuv4upr6iwu.txt