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Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
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Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Published on: March 23, 2022

Features of carnitine palmitoyltransferase type I deficiency

S E Olpin1, J Allen, J R Bonham

  • 1Neonatal Screening and Chemical Pathology, Sheffield Children's Hospital, UK.

Journal of Inherited Metabolic Disease
|April 5, 2001
PubMed

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