Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes ; volume:11 ; number:1 ; day:30 ; month:8 ; year:2024 ; pages:1-4 ; date:12.2024
Human genome variation ; 11, Heft 1 (30.8.2024), 1-4, 12.2024
- Urheber
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Mokhtari, Diana
Jahanpanah, Mohammad
Jabbari, Nasim
Azari, Hamed
Davarnia, Sana
Mokaber, Haleh
Arish, Sara
Molatefi, Rasol
Abbasi, Vahid
Davarnia, Behzad
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41439-024-00292-x
- URN
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urn:nbn:de:101:1-2411152100430.464920323653
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:24 MESZ
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Beteiligte
- Mokhtari, Diana
- Jahanpanah, Mohammad
- Jabbari, Nasim
- Azari, Hamed
- Davarnia, Sana
- Mokaber, Haleh
- Arish, Sara
- Molatefi, Rasol
- Abbasi, Vahid
- Davarnia, Behzad
- SpringerLink (Online service)
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