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Updated: Apr 17, 2026

06:48
Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
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[A case of β-ketothiolase deficiency caused by a ACAT1 gene variation with atypical biochemical phenotype]
1Department of Genetic Metabolism and Endocrinology, Wuhan Children's Hospital(Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430016, China.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|April 15, 2026
Abstract
No abstract available in PubMed .
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