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Updated: Aug 6, 2026

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Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
D-2-hydroxyglutaric aciduria: evidence of clinical and biochemical heterogeneity
L Wagner1, G F Hoffmann, C Jakobs
1Department of Metabolic Diseases, University Children's Hospital of Marburg, Germany.
Journal of Inherited Metabolic Disease
|August 1, 1998
Abstract
No abstract available in PubMed .
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