학술논문
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review.
Document Type
Article
Author
Source
Turkish Journal of Pediatrics; Nov/Dec2023, Vol. 65 Issue 6, p1018-1024, 7p, 1 Black and White Photograph, 1 Chart
Subject
Language
ISSN
00414301
Abstract
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