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A molecular explanation for the recessive nature of parkin-linked Parkinson’s disease

A molecular explanation for the recessive nature of parkin-linked Parkinson’s disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3709501

A molecular explanation for the recessive nature of parkin-linked Parkinson’s disease

About this item

Full title

A molecular explanation for the recessive nature of parkin-linked Parkinson’s disease

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2013-06, Vol.4 (1), p.1983-1983, Article 1983

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Mutations in the
park2
gene, encoding the RING-inBetweenRING-RING E3 ubiquitin ligase parkin, cause 50% of autosomal recessive juvenile Parkinsonism cases. More than 70 known pathogenic mutations occur throughout parkin, many of which cluster in the inhibitory amino-terminal ubiquitin-like domain, and the carboxy-terminal RING2 domain that is...

Alternative Titles

Full title

A molecular explanation for the recessive nature of parkin-linked Parkinson’s disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3709501

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3709501

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/ncomms2983

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