Reactome | Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features

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Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features Show undefined attributes

author	[Person:2426257] Unger, S [Person:3636848] Lausch, E [Person:3636845] Rossi, A [Person:2730971] Megarbane, A [Person:508086] Sillence, D [Person:3636851] Alcausin, M [Person:3636867] Aytes, A [Person:3636798] Mendoza-Londono, R [Person:3636814] Nampoothiri, S [Person:3636792] Afroze, B [Person:3636806] Hall, B [Person:3636820] Lo, IF [Person:3636846] Lam, ST [Person:3636842] Hoefele, J [Person:3636818] Rost, I [Person:3636802] Wakeling, E [Person:3636805] Mangold, E [Person:3636849] Godbole, K [Person:3636850] Vatanavicharn, N [Person:3636852] Franco, LM [Person:3636813] Chandler, K [Person:3636856] Hollander, S [Person:3636855] Velten, T [Person:3636819] Reicherter, K [Person:3636797] Spranger, J [Person:508045] Robertson, S [Person:2426322] Bonafe, L [Person:2426272] Zabel, B [Person:3621721] Superti-Furga, A
created	[InstanceEdit:3636794] Jassal, B, 2013-05-29
dbId	3636829
displayName	Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features
journal	Am. J. Med. Genet. A
modified	[InstanceEdit:5364052] D'Eustachio, Peter, 2014-04-19
pages	2543-9
pubMedIdentifier	20830804
schemaClass	LiteratureReference
title	Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: congenital dislocations and vertebral changes as principal diagnostic features
url	http://www.ncbi.nlm.nih.gov/pubmed/20830804
volume	152
year	2010

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