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Autor:
Heidi R Fuller, Berhan eMandefro, Sally L Shirran, Andrew R Gross, Anjoscha Samija Kaus, Catherine H Botting, Glenn E Morris, Dhruv eSareen
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2016)
Spinal muscular atrophy (SMA) is an inherited neuromuscular disease primarily characterized by degeneration of spinal motor neurons, and caused by reduced levels of the SMN protein. Previous studies to understand the proteomic consequences of reduced
Externí odkaz:
https://doaj.org/article/df5a2412124f4abbb23296861b2a14bc