Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts

Audrey O'Neill1, Cindy Bayer2, Emily McQuillen1

  • 1Ambry Genetics, Aliso Viejo, California, USA.

Summary

GCNT2-related cataracts are linked to variants in GCNT2. A new study identifies a disease-associated variant in exon 1B, suggesting its clinical relevance for congenital cataracts.

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