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4. CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia. Rizzu P; van Mil SE; Anar B; Rosso SM; Donker Kaat L; Heutink P; van Swieten JC Am J Med Genet B Neuropsychiatr Genet; 2006 Dec; 141B(8):944-6. PubMed ID: 16941655 [TBL] [Abstract][Full Text] [Related]
5. CHMP2B mutations are not a common cause of frontotemporal lobar degeneration. Cannon A; Baker M; Boeve B; Josephs K; Knopman D; Petersen R; Parisi J; Dickison D; Adamson J; Snowden J; Neary D; Mann D; Hutton M; Pickering-Brown SM Neurosci Lett; 2006 May; 398(1-2):83-4. PubMed ID: 16431024 [TBL] [Abstract][Full Text] [Related]
6. No association of chromatin-modifying protein 2B with sporadic frontotemporal dementia. Schumacher A; Friedrich P; Diehl-Schmid J; Ibach B; Eisele T; Laws SM; Förstl H; Kurz A; Riemenschneider M Neurobiol Aging; 2007 Nov; 28(11):1789-90. PubMed ID: 16979267 [TBL] [Abstract][Full Text] [Related]
7. CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro. van der Zee J; Urwin H; Engelborghs S; Bruyland M; Vandenberghe R; Dermaut B; De Pooter T; Peeters K; Santens P; De Deyn PP; Fisher EM; Collinge J; Isaacs AM; Van Broeckhoven C Hum Mol Genet; 2008 Jan; 17(2):313-22. PubMed ID: 17956895 [TBL] [Abstract][Full Text] [Related]
8. Six generations of CHMP2B-mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival. Roos P; Johannsen P; Lindquist SG; Brown JM; Waldemar G; Duno M; Nielsen TT; Budtz-Jørgensen E; Gydesen S; Holm IE; Collinge J; Isaacs AM; ; Nielsen JE Acta Neurol Scand; 2022 May; 145(5):529-540. PubMed ID: 34997757 [TBL] [Abstract][Full Text] [Related]