Availability: Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia:

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Main Authors:	Perez-Branguli, Francesc (Author), Mishra, Himanshu K. (Author), Prots, Iryna (Author), Havlicek, Steven (Author), Kohl, Zacharias (Author), Saul, Domenica (Author), Rummel, Christine (Author), Dorca-Arevalo, Jonatan (Author), Regensburger, Martin 1985- (Author), Graef, Daniela (Author), Sock, Elisabeth (Author), Blasi, Juan (Author), Groemer, Teja W. (Author), Schlötzer-Schrehardt, Ursula (Author), Winkler, Jürgen (Author), Winner, Beate (Author)
Format:	Electronic eBook
Language:	English
Published:	Erlangen Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) 2016
Links:	https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-74413 http://d-nb.info/111329082X/34 https://open.fau.de/handle/openfau/7441
Item Description:	Aus: Human Molecular Genetics 23.18 (2014): S. 4859-4874. <http://hmg.oxfordjournals.org/content/23/18/4859.abstract> Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence or a national licence (funded by the DFG, German Research Foundation) respectively.
Physical Description:	1 Online-Ressource
Format:	Langzeitarchivierung gewährleistet, LZA

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spelling	Perez-Branguli, Francesc Verfasser aut Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia Francesc Pérez-Brangulí ; Himanshu K. Mishra ; Iryna Prots ; Steven Havlicek ; Zacharias Kohl ; Domenica Saul ; Christine Rummel ; Jonatan Dorca-Arevalo ; Martin Regensburger ; Daniela Graef ; Elisabeth Sock ; Juan Blasi ; Teja W. Groemer ; Ursula Schlötzer-Schrehardt ; Jürgen Winkler ; Beate Winner Erlangen Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) 2016 1 Online-Ressource txt rdacontent c rdamedia cr rdacarrier Aus: Human Molecular Genetics 23.18 (2014): S. 4859-4874. <http://hmg.oxfordjournals.org/content/23/18/4859.abstract> Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence or a national licence (funded by the DFG, German Research Foundation) respectively. Langzeitarchivierung gewährleistet, LZA Mishra, Himanshu K. Verfasser aut Prots, Iryna Verfasser aut Havlicek, Steven Verfasser aut Kohl, Zacharias Verfasser aut Saul, Domenica Verfasser aut Rummel, Christine Verfasser aut Dorca-Arevalo, Jonatan Verfasser aut Regensburger, Martin 1985- Verfasser (DE-588)1017289719 aut Graef, Daniela Verfasser aut Sock, Elisabeth Verfasser aut Blasi, Juan Verfasser aut Groemer, Teja W. Verfasser aut Schlötzer-Schrehardt, Ursula Verfasser aut Winkler, Jürgen Verfasser aut Winner, Beate Verfasser aut https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-74413 Resolving-System kostenfrei Volltext http://d-nb.info/111329082X/34 Langzeitarchivierung Nationalbibliothek kostenfrei Volltext https://open.fau.de/handle/openfau/7441 Verlag kostenfrei Volltext
spellingShingle	Perez-Branguli, Francesc Mishra, Himanshu K. Prots, Iryna Havlicek, Steven Kohl, Zacharias Saul, Domenica Rummel, Christine Dorca-Arevalo, Jonatan Regensburger, Martin 1985- Graef, Daniela Sock, Elisabeth Blasi, Juan Groemer, Teja W. Schlötzer-Schrehardt, Ursula Winkler, Jürgen Winner, Beate Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
title	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
title_auth	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
title_exact_search	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
title_full	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia Francesc Pérez-Brangulí ; Himanshu K. Mishra ; Iryna Prots ; Steven Havlicek ; Zacharias Kohl ; Domenica Saul ; Christine Rummel ; Jonatan Dorca-Arevalo ; Martin Regensburger ; Daniela Graef ; Elisabeth Sock ; Juan Blasi ; Teja W. Groemer ; Ursula Schlötzer-Schrehardt ; Jürgen Winkler ; Beate Winner
title_fullStr	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia Francesc Pérez-Brangulí ; Himanshu K. Mishra ; Iryna Prots ; Steven Havlicek ; Zacharias Kohl ; Domenica Saul ; Christine Rummel ; Jonatan Dorca-Arevalo ; Martin Regensburger ; Daniela Graef ; Elisabeth Sock ; Juan Blasi ; Teja W. Groemer ; Ursula Schlötzer-Schrehardt ; Jürgen Winkler ; Beate Winner
title_full_unstemmed	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia Francesc Pérez-Brangulí ; Himanshu K. Mishra ; Iryna Prots ; Steven Havlicek ; Zacharias Kohl ; Domenica Saul ; Christine Rummel ; Jonatan Dorca-Arevalo ; Martin Regensburger ; Daniela Graef ; Elisabeth Sock ; Juan Blasi ; Teja W. Groemer ; Ursula Schlötzer-Schrehardt ; Jürgen Winkler ; Beate Winner
title_short	Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia
title_sort	dysfunction of spatacsin leads to axonal pathology in spg11 linked hereditary spastic paraplegia
url	https://nbn-resolving.org/urn:nbn:de:bvb:29-opus4-74413 http://d-nb.info/111329082X/34 https://open.fau.de/handle/openfau/7441
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