Identification and Functional Analysis of a Defect in the Human ALG9 Gene: Definition of Congenital Disorder of Glycosylation Type IL
- 1 July 2004
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 75 (1) , 146-150
- https://doi.org/10.1086/422367
Abstract
No abstract availableKeywords
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