Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: 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

Creator: Mokhtari, Diana
Jahanpanah, Mohammad
Jabbari, Nasim
Azari, Hamed
Davarnia, Sana
Mokaber, Haleh
Arish, Sara
Molatefi, Rasol
Abbasi, Vahid
Davarnia, Behzad

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41439-024-00292-x

URN: urn:nbn:de:101:1-2411152100430.464920323653

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

Last update: 15.08.2025, 7:24 AM CEST

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Associated

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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Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes

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Other Objects (12)

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