http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25416196

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contentType Case Reports|Journal Article|Research Support, Non-U.S. Gov't
endingPage 713
issn 0340-6199
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issueIdentifier 10
pageRange 710-713
publicationName European Journal of Pediatrics
startingPage 710
bibliographicCitation Neumann LM, von Moers A, Kunze J, Blankenstein O, Marquardt T. Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation. European Journal of Pediatrics. 2003 Aug 02;162(10):710–3. doi: 10.1007/s00431-003-1278-8.
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date 2003-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/12905014
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language English
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title Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation
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Total number of triples: 34.