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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.
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.
Area of Science:
- Genetics
- Ophthalmology
- Biochemistry
Background:
- GCNT2-related cataracts present as bilateral congenital cataracts (CC), potentially with the adult i blood phenotype.
- GCNT2 has three isoforms (1A, 1B, 1C), with exon 1C linked to the blood phenotype, but the role of other transcripts in CC is unclear.
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