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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism su...

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism su...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313541146

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

The genetics underlying the autism spectrum disorders (ASDs) is complex and remains poorly understood. Previous work has demonstrated an important role for structural variation in a subset of cases, but has lacked the resolution necessary to move beyond detection of large regions of potential interest to identification of individual genes. To pinpo...

Alternative Titles

Full title

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1313541146

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313541146

Other Identifiers

ISSN

1553-7404,1553-7390

E-ISSN

1553-7404

DOI

10.1371/journal.pgen.1000536

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