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Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly

Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ee12dfd404fa46c8ab3d32c0f81a6549

Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly

About this item

Full title

Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly

Publisher

England: BioMed Central Ltd

Journal title

Journal of orthopaedic surgery and research, 2024-07, Vol.19 (1), p.449-8, Article 449

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Polydactyly is a prevalent congenital anomaly with an incidence of 2.14 per 1000 live births in China. GLI family zinc finger 3 (GLI3) is a classical causative gene of polydactyly, and serves as a pivotal transcription factor in the hedgehog signaling pathway, regulating the development of the anterior-posterior axis in limbs.
Three pedigrees of...

Alternative Titles

Full title

Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_ee12dfd404fa46c8ab3d32c0f81a6549

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ee12dfd404fa46c8ab3d32c0f81a6549

Other Identifiers

ISSN

1749-799X

E-ISSN

1749-799X

DOI

10.1186/s13018-024-04928-0

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