Related Experiment Video
Updated: Jun 28, 2026

06:48
Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
Severe Tangier disease with a novel ABCA1 gene mutation
S Schippling1, M Orth, U Beisiegel
1Department of Neurology, University Medical Center Hamburg Eppendorf, Martinistr. 52, 20246 Hamburg, Germany. s.schippling@uke.uni-hamburg.de
Neurology
|October 29, 2008
Abstract
No abstract available in PubMed .
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