Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)
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Title
Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)
Authors
Keywords
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Journal
CLINICAL GENETICS
Volume 82, Issue 3, Pages 256-263
Publisher
Wiley
Online
2011-06-23
DOI
10.1111/j.1399-0004.2011.01745.x
References
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Related references
Note: Only part of the references are listed.- Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation
- (2011) Choong Yi Fong et al. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
- Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism
- (2011) Jin-Sung Park et al. HUMAN MUTATION
- ATP13A2-related neurodegeneration (PARK9) without evidence of brain iron accumulation
- (2011) Hsin Fen Chien et al. MOVEMENT DISORDERS
- Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome
- (2010) A. S. Al-Din et al. ACTA NEUROLOGICA SCANDINAVICA
- Recessively Inherited Parkinsonism
- (2010) Norbert Brüggemann et al. ARCHIVES OF NEUROLOGY
- Rapid screening of ATP13A2 variant with high-resolution melting analysis
- (2010) Manabu Funayama et al. MOVEMENT DISORDERS
- Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations
- (2010) Coro Paisán-Ruiz et al. MOVEMENT DISORDERS
- ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation
- (2010) Susanne A. Schneider et al. MOVEMENT DISORDERS
- Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability
- (2010) Lucio Santoro et al. NEUROGENETICS
- Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China
- (2010) Qing-Zhou Fei et al. NEUROSCIENCE LETTERS
- Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation
- (2010) David Crosiers et al. PARKINSONISM & RELATED DISORDERS
- ATP13A2variants in early-onset Parkinson's disease patients and controls
- (2009) Ana Djarmati et al. MOVEMENT DISORDERS
- ATP13A2 G2236A variant is rare in patients with early-onset Parkinson's disease and familial Parkinson's disease from mainland China
- (2009) X.-Y. Mao et al. PARKINSONISM & RELATED DISORDERS
- ATP13A2variability in Parkinson disease
- (2008) Carles Vilariño-Güell et al. HUMAN MUTATION
- Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
- (2008) C. H. Lin et al. NEUROLOGY
- PARK9-LINKED PARKINSONISM IN EASTERN ASIA: MUTATION DETECTION IN ATP13A2 AND CLINICAL PHENOTYPE
- (2008) Y. P. Ning et al. NEUROLOGY
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