Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients

Abstract Background The peroxisome is a ubiquitous single membrane-enclosed organelle with an important metabolic role. Peroxisomal disorders represent a class of medical conditions caused by deficiencies in peroxisome function and are segmented into enzyme-and-transporter defects (defects in single...

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Päätekijät:	Zhixing Zhu, Georgi Z. Genchev, Yanmin Wang, Wei Ji, Xiaofen Zhang, Hui Lu, Sira Sriswasdi, Guoli Tian
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	BMC 2023-05-01
Sarja:	Orphanet Journal of Rare Diseases
Aiheet:	X-linked adrenoleukodystrophy X-ALD Zellweger syndrome Very long chain fatty acids C26: carnitine Hexacosanoylcarnitine
Linkit:	https://doi.org/10.1186/s13023-023-02673-x
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