Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
| Errataetall: |
ErratumFor: Genet Med. 2022 Oct;24(10):2079-2090. - PMID 35986737 |
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| Medienart: |
E-Artikel |
| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:25 |
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| Enthalten in: |
Genetics in medicine : official journal of the American College of Medical Genetics - 25(2023), 10 vom: 03. Okt., Seite 100961 |
| Sprache: |
Englisch |
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| Links: |
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| Themen: |
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| Anmerkungen: |
Date Revised 06.03.2024 published: Print-Electronic ErratumFor: Genet Med. 2022 Oct;24(10):2079-2090. - PMID 35986737 Citation Status PubMed-not-MEDLINE |
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| doi: |
10.1016/j.gim.2023.100961 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| 245 | 1 | 0 | |a Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy |
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| 500 | |a ErratumFor: Genet Med. 2022 Oct;24(10):2079-2090. - PMID 35986737 | ||
| 500 | |a Citation Status PubMed-not-MEDLINE | ||
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