Myophosphorylase deficiency: An unusually severe form with myoglobinuria
- 30 September 1994
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 125 (3) , 409-410
- https://doi.org/10.1016/s0022-3476(05)83287-1
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Phosphorylase isoenzymes in normal and myophosphorylase‐deficient human heartNeurology, 1979
- Debrancher deficiency: Neuromuscular disorder in 5 adultsAnnals of Neurology, 1979
- Fatal infantile form of muscle phosphorylase deficiencyNeurology, 1978
- Dominant Inheritance of McArdle SyndromeArchives of Neurology, 1976
- A Family Study of Phosphorylase Deficiency in MuscleAnnals of Internal Medicine, 1965