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Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the SACS Gene Cover

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the SACS Gene

Open Access
|Jun 2020

Authors

Jindapa Srikajon

JindapaS@hotmail.com

Division of Neurology, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok

Yuvadee Pitakpatapee

yuvadee.pit@gmail.com

Division of Neurology, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok

Chanin Limwongse

chanin.lim@mahidol.ac.th

Division of Medical Genetics, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok

Niphon Chirapapaisan

niphon.chi@mahidol.ac.th

Department of Ophthalmology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok

Prachaya Srivanitchapoom

cloundbuffy@gmail.com

Division of Neurology, Department of Medicine, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok
DOI: https://doi.org/10.5334/tohm.68 | Journal eISSN: 2160-8288
Language: English
Submitted on: Jan 16, 2020
Accepted on: Apr 15, 2020
Published on: Jun 8, 2020
Published by: Ubiquity Press
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2020 Jindapa Srikajon, Yuvadee Pitakpatapee, Chanin Limwongse, Niphon Chirapapaisan, Prachaya Srivanitchapoom, published by Ubiquity Press
This work is licensed under the Creative Commons Attribution 4.0 License.