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Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parki...

Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parki...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_22647602

Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration

About this item

Full title

Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration

Publisher

United States: National Academy of Sciences

Journal title

Proceedings of the National Academy of Sciences - PNAS, 2012-06, Vol.109 (24), p.9611-9616

Language

English

Formats

Publication information

Publisher

United States: National Academy of Sciences

More information

Scope and Contents

Contents

Parkinson disease (PD) is a progressive neurodegenerative disorder pathologically characterized by the loss of dopaminergic neurons from the substantia nigra pars compacta and the presence, in affected brain regions, of protein inclusions named Lewy bodies (LBs). The ATP13A2 gene (locus PARK9) encodes the protein ATP13A2, a lysosomal type 5 P-type...

Alternative Titles

Full title

Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmed_primary_22647602

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_22647602

Other Identifiers

ISSN

0027-8424

E-ISSN

1091-6490

DOI

10.1073/pnas.1112368109

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