Parkinson's disease mutations in PINK1 result in decreased Complex I activity 
and deficient synaptic function

Morais, V. A.; Verstreken, P.; Roethig, A.; Smet, J.; Snellinx, A.; Vanbrabant, M.; Haddad, D.; Frezza, C.; Mandemakers, W.; Vogt-Weisenhorn, D.; Van Coster, R.; Wurst, W.; Scorrano, L.; De Strooper, B.

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Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function

Morais, V. A., Verstreken, P., Roethig, A., Smet, J., Snellinx, A., Vanbrabant, M., et al. (2009). Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function. EMBO Molecular Medicine, 1(2), 99-111.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-92AD-4 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-92AE-2

Genre: Journal Article

Alternative Title : EMBO Mol. Med.

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Creators:
Morais, V. A., Author
Verstreken, P., Author
Roethig, A., Author
Smet, J., Author
Snellinx, A., Author
Vanbrabant, M., Author
Haddad, D., Author
Frezza, C., Author
Mandemakers, W., Author
Vogt-Weisenhorn, D.¹, Author
Van Coster, R., Author
Wurst, W.², Author
Scorrano, L., Author
De Strooper, B., Author

Affiliations:
1AG Deussing, Jan, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607145
2Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137

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Free keywords: Complex I; mitochondrial dysfunction; Parkinson's disease; reserve pool deficit

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Language(s): eng - English

Dates: Date issued: 2009-05

Publication Status: Issued

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Table of Contents: -

Rev. Type: Peer

Identifiers: eDoc: 451189
ISI: 000273563000006

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Title: EMBO Molecular Medicine

Alternative Title : EMBO Mol. Med.

Source Genre: Journal

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Pages: - Volume / Issue: 1 (2) Sequence Number: - Start / End Page: 99 - 111 Identifier: ISSN: 1757-4676