Author:
Balakrishnan Bijina,Altassan Ruqaiah,Budhraja Rohit,Liou Willisa,Lupo Arielle,Bryant Sarah,Mankouski Anastasiya,Radenkovic Silvia,Preston Graeme J.,Pandey Akhilesh,Boudina Sihem,Kozicz Tamas,Morava Eva,Lai Kent
Subject
Biochemistry (medical),Public Health, Environmental and Occupational Health,General Medicine,Physiology (medical)
Reference43 articles.
1. Mutations in hereditary phosphoglucomutase 1 deficiency map to key regions of enzyme structure and function;Beamer;J Inherit Metab Dis,2015
2. Muscle glycogenosis due to phosphoglucomutase 1 deficiency;Stojkovic;N Engl J Med,2009
3. Glycogen storage disease-like phenotype with central nervous system involvement in a PGM1-CDG patient;Ondruskova;Neuro Endocrinol Lett,2014
4. PGM1 deficiency: substrate use during exercise and effect of treatment with galactose;Voermans;Neuromuscul Disord,2017
5. A case with rare type of congenital disorder of glycosylation: Pgm1-Cdg;Kucukcongar;Genet Couns,2015
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献