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Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
- Source :
-
Chinese medical journal [Chin Med J (Engl)] 2019 Jul 05; Vol. 132 (13), pp. 1615-1618. - Publication Year :
- 2019
- Subjects :
- Humans
Male
Middle Aged
Multiple Acyl Coenzyme A Dehydrogenase Deficiency physiopathology
Mutation genetics
Electron-Transferring Flavoproteins genetics
Iron-Sulfur Proteins genetics
Multiple Acyl Coenzyme A Dehydrogenase Deficiency genetics
Oxidoreductases Acting on CH-NH Group Donors genetics
Respiratory Insufficiency genetics
Rhabdomyolysis genetics
Rhabdomyolysis physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 2542-5641
- Volume :
- 132
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- Chinese medical journal
- Publication Type :
- Academic Journal
- Accession number :
- 31058673
- Full Text :
- https://doi.org/10.1097/CM9.0000000000000288