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Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f36d8250a6ce4896a0f38551711ec1ef

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Microphthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of eye malformations which play a role in childhood visual impairment. Although the predominant cause of eye malformations is known to be heritable in nature, with 80% of cases displaying loss-of-function mutations in the ocular developmental genes OTX2 or SOX2, t...

Alternative Titles

Full title

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_f36d8250a6ce4896a0f38551711ec1ef

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f36d8250a6ce4896a0f38551711ec1ef

Other Identifiers

ISSN

1741-7007

E-ISSN

1741-7007

DOI

10.1186/s12915-022-01475-0

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