Publications
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Filters: Author is Harshman, Lyndsay A and Keyword is Mannosyltransferases [Clear All Filters]
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients. Hum Mutat 37, 653-60 (2016).
Congenital nephrotic syndrome in an infant with ALG1-congenital disorder of glycosylation. Pediatr Int 58, 785-8 (2016).