학술논문
Case report: Thirty-year progression of an EMPF1 encephalopathy due to defective mitochondrial and peroxisomal fission caused by a novel de novo heterozygous DNM1L variant.
Document Type
Article
Author
Source
Frontiers in Neurology; 9/23/2022, Vol. 13, p1-9, 9p
Subject
Language
ISSN
16642295
Abstract
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