Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS.

Tassone, F; Greco, C M; Hunsaker, M R; Seritan, A L; Berman, R F; Gane, L W; Jacquemont, S; Basuta, K; Jin, L-W; Hagerman, P J; Hagerman, R J

Tassone, F; Greco, C M; Hunsaker, M R; Seritan, A L; Berman, R F; Gane, L W; Jacquemont, S; Basuta, K; Jin, L-W; Hagerman, P J; Hagerman, R J.

Affiliation

Tassone F; Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, USA. ftassone@ucdavis.edu

Genes Brain Behav ; 11(5): 577-85, 2012 Jul.

Article in En | MEDLINE | ID: mdl-22463693

Subject(s)

Ataxia/genetics; Brain/pathology; Dementia/genetics; Fragile X Mental Retardation Protein/genetics; Fragile X Syndrome/genetics; Tremor/genetics; Aged; Aged, 80 and over; Alleles; Ataxia/pathology; Dementia/pathology; Female; Fragile X Syndrome/pathology; Humans; Intranuclear Inclusion Bodies/genetics; Intranuclear Inclusion Bodies/pathology; Middle Aged; Neurons/pathology; Syndrome; Tremor/pathology

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Full text: 1 Database: MEDLINE Main subject: Ataxia / Tremor / Brain / Dementia / Fragile X Mental Retardation Protein / Fragile X Syndrome Limits: Aged / Aged80 / Female / Humans / Middle aged Language: En Year: 2012 Type: Article

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