학술논문

A milder form of molybdenum cofactor deficiency type A presenting as Leigh's syndrome-like phenotype highlighting the secondary mitochondrial dysfunction: a case report.
Document Type
Article
Source
Frontiers in Neurology; 2023, p01-06, 6p
Subject
MOLYBDENUM
PHENOTYPES
PHENOTYPIC plasticity
MITOCHONDRIA
URIC acid
MITOCHONDRIAL pathology
Language
ISSN
16642295
Abstract
Copyright of Frontiers in Neurology is the property of Frontiers Media S.A. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)