Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree ; volume:19 ; number:1 ; day:25 ; month:11 ; year:2024 ; pages:1-9 ; date:12.2024
Orphanet journal of rare diseases ; 19, Heft 1 (25.11.2024), 1-9, 12.2024

Creator: Guo, Zhenglong
Huo, Dawei
Shao, Yingying
Yang, Wenke
Wang, Jinming
Zhang, Yuwei
Xiao, Hai
Hao, Bingtao
Liao, Shixiu

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13023-024-03465-7

URN: urn:nbn:de:101:1-2502102120567.309780005324

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

Last update: 15.08.2025, 7:34 AM CEST

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Guo, Zhenglong
Huo, Dawei
Shao, Yingying
Yang, Wenke
Wang, Jinming
Zhang, Yuwei
Xiao, Hai
Hao, Bingtao
Liao, Shixiu
SpringerLink (Online service)

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Novel biallelic variants in IREB2 cause an early-onset neurodegenerative disorder in a Chinese pedigree

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