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Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
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[Mitochondrial acetoacetyl-CoA thiolase deficiency: neonatal onset]

I Cubillo Serna1, J Suárez Fernández, J M Merino Arribas

  • 1Unidad de Neonatología, Servicio de Pediatría, Hospital General Yagüe, Burgos, España. cibercubi@hotmail.com

Anales De Pediatria (Barcelona, Spain : 2003)
|October 24, 2007
PubMed

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