Mutation at the SCA17 locus is not a common cause of parkinsonism-Reference-Cited by-同舟云学术

Mutation at the SCA17 locus is not a common cause of parkinsonism

Published:2003-08 Issue:6 Volume:9 Page:317-320
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Hernandez Dena,Hanson Melissa,Singleton Amanda,Gwinn-Hardy Katrina,Freeman Jason,Ravina Bernard,Doheny Dana,Gallardo Marisol,Weiser Roberto,Hardy John,Singleton Andrew

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference19 articles.

1. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein;Nakamura;Hum Mol Genet,2001

2. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10;Matsuura;Nat Genet,2000

3. Glutamine repeats and neurodegenerative diseases;Perutz;Brain Res Bull,1999

4. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12;Holmes;Nat Genet,1999

5. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr;Nat Genet,1993

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1. Genotype–Phenotype Correlations for ATX‐ TBP ( SCA17 ): MDSGene Systematic Review;Movement Disorders;2022-11-14

2. Parkinsonism in Spinocerebellar Ataxia;BioMed Research International;2015

3. Investigating function and connectivity of morphometric findings — Exemplified on cerebellar atrophy in spinocerebellar ataxia 17 (SCA17);NeuroImage;2012-09

4. PET and MRI Reveal Early Evidence of Neurodegeneration in Spinocerebellar Ataxia Type 17;Journal of Nuclear Medicine;2012-05-31

5. Movement disorders in spinocerebellar ataxias;Movement Disorders;2011-03-02