Molybdenum cofactor deficiency type B manifested as Leigh-like syndrome : a case report and literature review

Objective: To explore the phenotypes and genotypes of molybdenum cofactor deficiency type B (MoCD-B) manifested as Leigh-like syndrome. Methods: The clinical data, laboratory tests, neuroimaging and gene results of one patient diagnosed as MoCD-B at Beijing Children's Hospital and Hebei Childre...

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Veröffentlicht in:	Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 59(2021), 2 vom: 02. Feb., Seite 119-124
1. Verfasser:	Tian, X J (VerfasserIn)
Weitere Verfasser:	Li, X, Fang, F, Liu, Z M, Wu, W J, Liu, K, Sun, S Z
Format:	Online-Aufsatz
Sprache:	Chinese
Veröffentlicht:	2021
Zugriff auf das übergeordnete Werk:	Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:	Case Reports Journal Article Review