Diagnosis of Peroxisomal Disorders

Journal of Pediatric Neurology 2020; 18(01): 053
DOI: 10.1055/s-0039-1692137

Letter to the Editor

Georg Thieme Verlag KG Stuttgart · New York

Authors

Beuy Joob

¹Medical Center Department, Sanitation 1, Medical Academic Center, Bangkok, Thailand
Viroj Wiwanitkit

²Department of Biological Science, Joseph Ayo Babalola University, Ikeji-Arakeji, Nigeria

References
1 Angurana SK, Suthar R, Panigrahi I. Peroxisomal disorders: experience from a genetic center in North India. J Pediatr Neurol 2019; 17 (02) 65-70
2 Braverman NE, Raymond GV, Rizzo WB. , et al. Peroxisome biogenesis disorders in the Zellweger spectrum: an overview of current diagnosis, clinical manifestations, and treatment guidelines. Mol Genet Metab 2016; 117 (03) 313-321
3 Takashima S, Saitsu H, Shimozawa N. Expanding the concept of peroxisomal diseases and efficient diagnostic system in Japan. J Hum Genet 2019; 64 (02) 145-152
4 Wanders RJ, Klouwer FC, Ferdinandusse S, Waterham HR, Poll-Thé BT. Clinical and laboratory diagnosis of peroxisomal disorders. Methods Mol Biol 2017; 1595: 329-342