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CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and seq...

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and seq...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1664201948

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

Publication information

Publisher

England: Elsevier Ltd

More information

Scope and Contents

Contents

Summary Background Identification of causative genes in mendelian forms of Parkinson's disease is valuable for understanding the cause of the disease. We did genetic studies in a Japanese family with autosomal dominant Parkinson's disease to identify novel causative genes. Methods We did a genome-wide linkage analysis on eight affected and five una...

Alternative Titles

Full title

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1664201948

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1664201948

Other Identifiers

ISSN

1474-4422

E-ISSN

1474-4465

DOI

10.1016/S1474-4422(14)70266-2

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