Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts. O'Neill A, Bayer C, McQuillen E, Smith ED, et al. Am J Med Genet A 2026 Mar 11. doi: 10.1002/ajmg.a.70123.

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O'Neill A, Bayer C, McQuillen E, Smith ED, et al. Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts. Am J Med Genet A 2026 Mar 11. doi: 10.1002/ajmg.a.70123.
PMID: 41813616