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ALG3-CDG: a Patient with Novel Variants and Review of the Genetic and Ophthalmic Findings.

Farolfi Martina,Cechova Anna,Ondruskova Nina,Zidkova Jana,Kousal Bohdan,Hansikova Hana,Honzik Tomas, Charles University and General University Hospital in Prague

BMC Ophthalmology(2021)

Cited 3|Views3
Key words
N-linked glycosylation,Congenital disorder of glycosylation,ALG3-CDG,Optic nerve hypoplasia,Arthrogryposis,Transferrin isoelectric focusing,Novel mutation
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