POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2377
- 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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POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype ; volume:10 ; number:1 ; day:3 ; month:5 ; year:2010 ; pages:1-10 ; date:12.2010
BMC neurology ; 10, Heft 1 (3.5.2010), 1-10, 12.2010
- Urheber
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Komulainen, Tuomas
- Beteiligte Personen und Organisationen
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Hinttala, Reetta
Kärppä, Mikko
Pajunen, Leila
Finnilä, Saara
Tuominen, Hannu
Rantala, Heikki
Hassinen, Ilmo
Majamaa, Kari
Uusimaa, Johanna
SpringerLink (Online service)
- DOI
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10.1186/1471-2377-10-29
- URN
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urn:nbn:de:1111-2016030328284
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
23.08.2025, 08:36 MESZ
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Beteiligte
- Komulainen, Tuomas
- Hinttala, Reetta
- Kärppä, Mikko
- Pajunen, Leila
- Finnilä, Saara
- Tuominen, Hannu
- Rantala, Heikki
- Hassinen, Ilmo
- Majamaa, Kari
- Uusimaa, Johanna
- SpringerLink (Online service)
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