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. 1992 Jul;29(7):514.

Chromosomes 14 and 21 as possible candidates for mapping the gene for Sanfilippo disease type IIIC.

J Zaremba ¹, W J Kleijer ¹, J G Huijmans ¹, B Poorthuis ¹, E Fidzianska ¹, I Glogowska ¹

PMCID: PMC1016036 PMID: 1640438

514

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Hopwood J. J., Elliott H. The diagnosis of the Sanfilippo C syndrome, using monosaccharide and oligosaccharide substrates to assay acetyl-CoA: 2-amino-2-deoxy-alpha-glucoside N-acetyltransferase activity. Clin Chim Acta. 1981 Apr 27;112(1):67–75. doi: 10.1016/0009-8981(81)90269-2. [DOI] [PubMed] [Google Scholar]
Kleijer W. J., Huijmans J. G., Blom W., Gorska D., Kubalska J., Walasek M., Zaremba J. Prenatal diagnosis of Sanfilippo disease type B. Hum Genet. 1984;66(4):287–288. doi: 10.1007/BF00287628. [DOI] [PubMed] [Google Scholar]

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