reference/13807687

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	7
issn	0002-9297
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pageRange	810-7
publicationName	American journal of human genetics
startingPage	810
bibliographicCitation	Tan J, Dunn J, Jaeken J, Schachter H. Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development. Am J Hum Genet. 1996 Oct;59(4):810–7. PMID: 8808595; PMCID: PMC1914797.
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date	199610
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC1914797 https://pubmed.ncbi.nlm.nih.gov/8808595
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development
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