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Article

Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion.

Ophthalmic genetics - 1 Feb 2022

Hemmati Sara, Khakpour Golnaz, Nadjafi-Semnani Fatemeh, Gordiz Arzhang, Sajadi Masoome, Abdi Fatemeh

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Share to Methylenetetrahydrofolate Reductase (NADPH2)

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Identifiers

PMID: 35232319
DOI: 10.1080/13816810.2022.2042701

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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