Phenotype of ST3GAL3 deficient patients: A case and review of the literature-Reference-Cited by-同舟云学术

Phenotype of ST3GAL3 deficient patients: A case and review of the literature

Published:2021-08 Issue:8 Volume:64 Page:104250
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Khamirani Hossein Jafari,Zoghi Sina,Faghihi Fatemeh,Dastgheib Seyed Alireza,Hassanipour Hamidreza,Bagher Tabei Seyed Mohammad,Mohammadi Sanaz,Masoudi Marjan,Poorang Shiva,Ehsani Elham,Dianatpour Mehdi

Funder

Shiraz University of Medical Sciences

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference23 articles.

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2. Sialosignaling: sialyltransferases as engines of self-fueling loops in cancer progression;Dall'Olio;Biochim. Biophys. Acta Gen. Subj.,2014

3. Levels of salivary sialic acid in children with autism spectrum disorder; could it Be related to stereotypes and hyperactivity?;Demirci;Clin. Psychopharmacol. Neurosci. Off. Sci. J. Korean Coll. Neuropsychopharmacol.,2019

4. Modulation of voltage-gated ion channels by sialylation;Ednie;Comp. Physiol.,2012

5. West syndrome caused by ST3Gal-III deficiency;Edvardson;Epilepsia,2013

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