Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
- 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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Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31) ; volume:9 ; number:1 ; day:21 ; month:7 ; year:2008 ; pages:1-4 ; date:12.2008
BMC medical genetics ; 9, Heft 1 (21.7.2008), 1-4, 12.2008
- Urheber
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Schlang, Katharina J.
- Beteiligte Personen und Organisationen
- DOI
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10.1186/1471-2350-9-71
- URN
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urn:nbn:de:1111-2016021835642
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:32 MESZ
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Beteiligte
- Schlang, Katharina J.
- Arning, Larissa
- Epplen, Jörg T.
- Stemmler, Susanne
- SpringerLink (Online service)
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