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pro vyhledávání: '"Rabea Betten"'
Autor:
Stefan Hauser, Marion Poenisch, Yvonne Schelling, Philip Höflinger, Stefanie Schuster, Axel Teegler, Rabea Betten, Jan-Åke Gustafsson, Jeannette Hübener-Schmid, Thomas Schlake, Frédéric Chevessier-Tünnesen, Nigel Horscroft, Ingemar Björkhem, Ludger Schöls
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss , Pp 359-370 (2019)
Hereditary spastic paraplegia type 5 is a neurodegenerative disease caused by loss-of-function mutations in the CYP7B1 gene encoding the oxysterol 7-α-hydroxylase involved in bile acid synthesis in the liver. Lack of CYP7B1 leads to an accumulation
Externí odkaz:
https://doaj.org/article/4aeaa97d4bae48d099f191ccf0272017
Autor:
Jan-Åke Gustafsson, Ingemar Björkhem, Stefanie Schuster, Yvonne Schelling, Frédéric Chevessier-Tünnesen, Axel Teegler, Ludger Schöls, Nigel Horscroft, Thomas Schlake, Jeannette Hübener-Schmid, Rabea Betten, Stefan Hauser, Philip Höflinger, Marion Poenisch
Publikováno v:
Molecular therapy 15, 359-370 (2019). doi:10.1016/j.omtm.2019.10.011
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 359-370 (2019)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 359-370 (2019)
Molecular Therapy. Methods & Clinical Development
Hereditary spastic paraplegia type 5 is a neurodegenerative disease caused by loss-of-function mutations in the CYP7B1 gene encoding the oxysterol 7-α-hydroxylase involved in bile acid synthesis in the liver. Lack of CYP7B1 leads to an accumulation