Monogenic mysteries unravel mitochondrial mechanisms

Autor:	Siri Lynne Rydning, Iselin M Wedding
Rok vydání:	2021
Předmět:	0301 basic medicine 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Humans Neurology (clinical) Computational biology Mitochondrion Biology 030217 neurology & neurosurgery Mitochondria
Zdroj:	Brain. 144:1286-1288
ISSN:	1460-2156 0006-8950
DOI:	10.1093/brain/awab098
Popis:	This scientific commentary refers to ‘Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia’, by Rebelo et al. (doi: 10.1093/brain/awab071).
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02607fd06cdd72e03bf1106969fbe8e3 https://doi.org/10.1093/brain/awab098 Zobrazit plný text záznamu