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Alexandra Mc Cullough Selected Research

Congenital disorder of glycosylation type 1G

11/2021A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum.

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Alexandra Mc Cullough Research Topics

Disease

1Congenital disorder of glycosylation type 1G
11/2021
1Metabolic Diseases (Metabolic Disease)
11/2021

Drug/Important Bio-Agent (IBA)

1MannosyltransferasesIBA
11/2021