William Dobyns to Congenital Disorders of Glycosylation
This is a "connection" page, showing publications William Dobyns has written about Congenital Disorders of Glycosylation.
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0.213
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SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals. Hum Mutat. 2019 07; 40(7):908-925.
Score: 0.176
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Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I. J Neurol. 1996 Oct; 243(10):700-5.
Score: 0.037