Associated Papers
A rare case of myopathy with fatigability due to PYROXD1 variation.
Baskar D et al.
Journal of Neuromuscular Diseases, 2025
Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey.
Daimagüler HS et al.
American Journal of Medical Genetics. Part A, 2021
Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencing.
Woods JD et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology, 2020
32037607 (PubMed )
Supplement: NEUP-40-302-s001.zip › NEUP_12641_Patient_Table_Redux.pdf
Clinical, histological, and genetic characterization of PYROXD1-related myopathy.
Lornage X et al.
Acta Neuropathologica Communications, 2019
Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy.
Sainio MT et al.
Journal of Neurology, 2019
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