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Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy: e1004111

Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy: e1004111

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1516742371

Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy: e1004111

About this item

Full title

Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy: e1004111

Publisher

San Francisco: Public Library of Science

Journal title

PLoS genetics, 2014-02, Vol.10 (2)

Language

English

Formats

Publication information

Publisher

San Francisco: Public Library of Science

More information

Scope and Contents

Contents

Cone-rod homeobox (CRX) protein is a "paired-like" homeodomain transcription factor that is essential for regulating rod and cone photoreceptor transcription. Mutations in human CRX are associated with the dominant retinopathies Retinitis Pigmentosa (RP), Cone-Rod Dystrophy (CoRD) and Leber Congenital Amaurosis (LCA), with variable severity. Hetero...

Alternative Titles

Full title

Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy: e1004111

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1516742371

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1516742371

Other Identifiers

ISSN

1553-7390

E-ISSN

1553-7404

DOI

10.1371/journal.pgen.1004111

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