Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia ; volume:20 ; number:1 ; day:4 ; month:7 ; year:2019 ; pages:1-6 ; date:12.2019
BMC medical genetics ; 20, Heft 1 (4.7.2019), 1-6, 12.2019
- Urheber
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Wakil, Salma M.
Alhissi, Safa
Dossari, Haya Al
Alqahtani, Ayesha
Shibin, Sherin
Melaiki, Brahim T.
Finsterer, Josef
Al-Hashem, Amal
Bohlega, Saeed
Alazami, Anas M.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12881-019-0851-6
- URN
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urn:nbn:de:101:1-2019121006145010189140
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:49 MESZ
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Beteiligte
- Wakil, Salma M.
- Alhissi, Safa
- Dossari, Haya Al
- Alqahtani, Ayesha
- Shibin, Sherin
- Melaiki, Brahim T.
- Finsterer, Josef
- Al-Hashem, Amal
- Bohlega, Saeed
- Alazami, Anas M.
- SpringerLink (Online service)
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