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pro vyhledávání: '"Sandra Müßig"'
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102059- (2020)
Bi-allelic loss-of-function mutations in the gene encoding the motor protein KIF1C are associated with Hereditary Spastic Paraplegia (HSP) type SPG58, a slowly progressive neurodegenerative motoneuron disease. The biological role of KIF1C is incomple
Externí odkaz:
https://doaj.org/article/b57ece3dcdc4429f8d69ceac27780be4
