ArticleHuman molecular genetics2016
A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.
Barden Chan et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleHuman molecular genetics2016
Barden Chan et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.