Phenotypic features of carbohydrate sulfotransferase 3 (CHST3) deficiency in 24 patients: Congenital dislocations and vertebral changes as principal diagnostic features-Reference-Cited by-同舟云学术

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

Published:2010-09-09 Issue:10 Volume:152A Page:2543-2549
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Unger Sheila,Lausch Ekkehart,Rossi Antonio,Mégarbané Andre,Sillence David,Alcausin Melanie,Aytes Antonio,Mendoza-Londono Roberto,Nampoothiri Sheela,Afroze Bushra,Hall Bryan,Lo Ivan F.M.,Lam Stephen T.S.,Hoefele Julia,Rost Imma,Wakeling Emma,Mangold Elisabeth,Godbole Komudi,Vatanavicharn Nithiwat,Franco Luis M.,Chandler Kate,Hollander Sophia,Velten Tanja,Reicherter Kerstin,Spranger Jürgen,Robertson Stephen,Bonafé Luisa,Zabel Bernhard,Superti-Furga Andrea

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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3. Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis;Hermanns;Am J Hum Genet,2008

4. Developmental regulation of the sulfation profile of chondroitin sulfate chains in the chicken embryo brain;Kitagawa;J Biol Chem,1997

5. Humero-spinal dysostosis with congenital heart disease;Kozlowski;Am J Dis Child,1974

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