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23. FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome. Buijsen RA; Sellier C; Severijnen LA; Oulad-Abdelghani M; Verhagen RF; Berman RF; Charlet-Berguerand N; Willemsen R; Hukema RK Acta Neuropathol Commun; 2014 Nov; 2():162. PubMed ID: 25471011 [TBL] [Abstract][Full Text] [Related]
24. [Neurodevelopmental (fragile X syndrome) and neurodegenerative (tremor/ataxia syndrome) disorders associated to the 'growth' of a gene]. Castro-Volio I; Cuenca-Berger P Rev Neurol; 2005 Apr 1-15; 40(7):431-7. PubMed ID: 15849678 [TBL] [Abstract][Full Text] [Related]
38. Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene. Loesch DZ; Sherwell S; Kinsella G; Tassone F; Taylor A; Amor D; Sung S; Evans A Clin Genet; 2012 Jul; 82(1):88-92. PubMed ID: 21476992 [TBL] [Abstract][Full Text] [Related]