Bi-allelic mutations in NDUFA6 establish its role in early-onset isolated mitochondrial complex I deficiency
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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In: American journal of human genetics, Volume 103.2018, Nr. 4, S. 592-601, doi:10.1016/j.ajhg.2018.08.013
- Ereignis
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Veröffentlichung
- (wo)
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Frankfurt am Main
- (wer)
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Universitätsbibliothek Johann Christian Senckenberg
- (wann)
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2018
- Urheber
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Alston, Charlotte
Heidler, Juliana
Dibley, Marris G.
Kremer, Laura S.
Taylor, Lucie S.
Fratter, Carl
French, Courtney E.
Glasgow, Ruth I. C.
Feichtinger, René G.
Delon, Isabelle
Pagnamenta, Alistair T.
Dolling, Helen
Lemonde, Hugh
Aiton, Neil
Bjornstad, Alf
Henneke, Lisa
Gärtner, Jutta
Thiele, Holger
Tauchmannova, Katerina
Quaghebeur, Gerardine
Houstek, Josef
Sperl, Wolfgang
Raymond, Lucy
Prokisch, Holger
Mayr, Johannes A.
McFarland, Robert
Poulton, Joanna
Ryan, Michael T.
Wittig, Ilka
Henneke, Marco
Taylor, Robert W.
- URN
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urn:nbn:de:hebis:30:3-477101
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:56 MEZ
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Beteiligte
- Alston, Charlotte
- Heidler, Juliana
- Dibley, Marris G.
- Kremer, Laura S.
- Taylor, Lucie S.
- Fratter, Carl
- French, Courtney E.
- Glasgow, Ruth I. C.
- Feichtinger, René G.
- Delon, Isabelle
- Pagnamenta, Alistair T.
- Dolling, Helen
- Lemonde, Hugh
- Aiton, Neil
- Bjornstad, Alf
- Henneke, Lisa
- Gärtner, Jutta
- Thiele, Holger
- Tauchmannova, Katerina
- Quaghebeur, Gerardine
- Houstek, Josef
- Sperl, Wolfgang
- Raymond, Lucy
- Prokisch, Holger
- Mayr, Johannes A.
- McFarland, Robert
- Poulton, Joanna
- Ryan, Michael T.
- Wittig, Ilka
- Henneke, Marco
- Taylor, Robert W.
- Universitätsbibliothek Johann Christian Senckenberg
Entstanden
- 2018
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