Associated Papers
Expanding the phenotype, genotype and biochemical knowledge of ALG3-CDG.
Alsharhan H et al.
Journal of Inherited Metabolic Disease, 2021
ALG3-CDG: a patient with novel variants and review of the genetic and ophthalmic findings.
Farolfi M et al.
Bmc Ophthalmology, 2021
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy.
Barba C et al.
Developmental Medicine and Child Neurology, 2016
Select a paper to view details