https://www.selleckchem.com/pr....oducts/gc7-sulfate.h
An amendment to this paper has been published and can be accessed via a link at the top of the paper. Inherited axonopathies (IA) are rare, clinically and genetically heterogeneous diseases that lead to length-dependent degeneration of the long axons in central (hereditary spastic paraplegia [HSP]) and peripheral (Charcot-Marie-Tooth type 2 [CMT2]) nervous systems. Mendelian high-penetrance alleles in over 100 different genes have been shown to cause IA; however, about 50% of IA cases do not receive a genetic diagnosis. A more compr
Curtir
Comentario
Compartilhar
