Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation

scientific article published on 12 February 2011

Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.EJPN.2011.01.001
P698PubMed publication ID21316993

P50authorChristine KleinQ21257320
Thomas SchwarzbraunQ56328568
Finbar O'CallaghanQ73091296
P2093author name stringChoong Yi Fong
Arndt Rolfs
P433issue3
P921main subjectparkinsonian syndromeQ1531991
heterozygosityQ124059385
P304page(s)271-275
P577publication date2011-02-12
P1433published inEuropean Journal of Paediatric NeurologyQ15755269
P1476titleJuvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation
P478volume15

Reverse relations

cites work (P2860)
Q28116203ATP13A2 and Alpha-synuclein: a Metal Taste in Autophagy
Q34774337ATP13A2/PARK9 Deficiency Neither Cause Lysosomal Impairment Nor Alter α-Synuclein Metabolism in SH-SY5Y Cells
Q36748089Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts
Q50248457Genetic analysis of the ATP1B4 gene in Chinese Han patients with Parkinson's disease
Q35175069Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death
Q34100399Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review

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