IARS2 mutations lead to Leigh syndrome with a combined oxidative phosphorylation deficiency

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: IARS2 mutations lead to Leigh syndrome with a combined oxidative phosphorylation deficiency ; volume:19 ; number:1 ; day:21 ; month:8 ; year:2024 ; pages:1-11 ; date:12.2024
Orphanet journal of rare diseases ; 19, Heft 1 (21.8.2024), 1-11, 12.2024

Creator: Dong, Qiyu
Yin, Xiaojie
Fan, Shuanglong
Zhong, Sheng
Yang, Wenxin
Chen, Keer
Wang, Qian
Ma, Xue
Mahlatsi, Refiloe Laurentinah
Yang, Yanling
Lyu, Jianxin
Fang, Hezhi
Wang, Ya

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-024-03310-x

URN: urn:nbn:de:101:1-2411072113344.172169929348

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:32 AM CEST

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Associated

Dong, Qiyu
Yin, Xiaojie
Fan, Shuanglong
Zhong, Sheng
Yang, Wenxin
Chen, Keer
Wang, Qian
Ma, Xue
Mahlatsi, Refiloe Laurentinah
Yang, Yanling
Lyu, Jianxin
Fang, Hezhi
Wang, Ya
SpringerLink (Online service)

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IARS2 mutations lead to Leigh syndrome with a combined oxidative phosphorylation deficiency

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Other Objects (12)

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