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Article

Corneal involvement in a case of autosomal dominant Stargardt-like macular dystrophy (STGD3) with ELOVL4 mutation.

Ophthalmic genetics - 1 Feb 2022

Zhai Yi, Benson Matthew D, MacDonald Ian M

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Identifiers

PMID: 34596007
DOI: 10.1080/13816810.2021.1983848

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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Corneal involvement in a case of autosomal dominant Stargardt-like macular dystrophy (STGD3) with ELOVL4 mutation.PMID 34596007Read ↗

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A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy.Semantic proximity Read ↗

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