3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects
- 31 December 1992
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 121 (6) , 940-942
- https://doi.org/10.1016/s0022-3476(05)80348-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Organic aciduria in Pearson syndromeEuropean Journal of Pediatrics, 1991
- Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficienciesVirchows Archiv, 1991
- Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndromeGenomics, 1991
- Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduriaThe Journal of Pediatrics, 1991
- Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.Journal of Clinical Investigation, 1990
- Juvenile Pearson SyndromeJournal of Child Neurology, 1990
- A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunctionPublished by Elsevier ,1979