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of 3
pro vyhledávání: '"SPG11/Spatacsin"'
Autor:
Susanna Cogo, James E. Tomkins, Nikoleta Vavouraki, Veronica Giusti, Federica Forcellato, Cinzia Franchin, Isabella Tessari, Giorgio Arrigoni, Laura Cendron, Claudia Manzoni, Laura Civiero, Patrick A. Lewis, Elisa Greggio
Publikováno v:
Neurobiology of Disease, Vol 174, Iss , Pp 105858- (2022)
Mutations in SPG11, encoding spatacsin, constitute the major cause of autosomal recessive Hereditary Spastic Paraplegia (HSP) with thinning of the corpus callosum. Previous studies showed that spatacsin orchestrates cellular traffic events through th
Externí odkaz:
https://doaj.org/article/44f7aee8cceb414d95b4e9e6dd924b2f
Akademický článek
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Autor:
Giorgio Arrigoni, James E. Tomkins, Federica Forcellato, Laura Civiero, Nikoleta Vavouraki, Patrick A. Lewis, Laura Cendron, Elisa Greggio, Isabella Tessari, Susanna Cogo, Cinzia Franchin, Claudia Manzoni
Mutations in SPG11, encoding spatacsin, constitute the major cause of autosomal recessive Hereditary Spastic Paraplegia (HSP) with thinning of the corpus callosum. Previous studies showed that spatacsin orchestrates cellular traffic events through th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e79da9413b2dd5b9309b1c1188b542c
https://doi.org/10.1101/2020.09.09.289009
https://doi.org/10.1101/2020.09.09.289009
