Article info
PDFBiochemical genetics
Original research
Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency
- Correspondence to Professor Barbara Plecko, Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria; barbara.plecko{at}medunigraz.at; Dr Katta M Girisha, Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India; girish.katta{at}manipal.edu
Citation
Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency
Publication history
- Received June 28, 2021
- Accepted October 31, 2021
- First published December 16, 2021.
Online issue publication
November 15, 2022
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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.