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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide associati...

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide associati...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4828586

Publication information

Publisher

England: Elsevier Ltd

More information

Scope and Contents

Contents

Summary Background Parkinson's disease has been reported in a small number of patients with chromosome 22q11.2 deletion syndrome. In this study, we screened a series of large, independent Parkinson's disease case-control studies for deletions at 22q11.2. Methods We used data on deletions spanning the 22q11.2 locus from four independent case-control...

Alternative Titles

Full title

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4828586

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4828586

Other Identifiers

ISSN

1474-4422

E-ISSN

1474-4465

DOI

10.1016/S1474-4422(16)00071-5

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