Abstract
Recent advances in instrumentation and technology have led to the identification of seven inherited metabolic diseases linked to a defect in phospholipid and glycosphingolipid biosynthesis. Analysis of patients’ plasma lipidomes can provide a valuable approach for detecting and monitoring diseases and the efficacy of their treatment [1].
Cite
CITATION STYLE
APA
Lamari, F., Sedel, F., & Saudubray, J. M. (2012). Disorders of phospholipid and glycosphingolipid synthesis. In Inborn Metabolic Diseases: Diagnosis and Treatment (pp. 485–495). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-15720-2_35
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