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Items: 2

1.
ST3GAL5-related disorders: a deficiency in ganglioside metabolism and a genetic cause of intellectual disability and choreoathetosis.
Eliza Gordon-Lipkin, Julie S. Cohen, Siddharth Srivastava, Bruno P. Soares, Eric Levey, Ali Fatemi
J Child Neurol. Author manuscript; available in PMC 2019 Nov 1.
Published in final edited form as: J Child Neurol. 2018 Nov; 33(13): 825–831. Published online 2018 Sep 5. doi: 10.1177/0883073818791099
PMCID:
PMC6188822
AbstractArticlePDF–180K
2.
Identification and Functional Characterization of ST3GAL5 and ST8SIA1 Variants in Patients with Thyroid-Associated Ophthalmopathy
Hyo Jin Park, Ju Hee Kim, Jin Sook Yoon, Yang Ji Choi, Yoon-Hee Choi, Koung Hoon Kook, Ji Ha Choi
Yonsei Med J. 2017 Nov 1; 58(6): 1160–1169. Published online 2017 Sep 28. doi: 10.3349/ymj.2017.58.6.1160
PMCID:
PMC5653481
AbstractArticlePDF–782K

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