SMN is required for dynamic relocalization of methylated nucleolar proteins during skeletal muscle differentiation

Benoit F Paquette
Deletions or loss-of-function mutations in the Survival of Motor Neuron 1 (Smn1) gene in humans is responsible for Spinal Muscular Atrophy (SMA), one of the leading genetic causes of infant mortality. The pathological hallmarks of this disease include the degeneration of lower motor neurons in the anterior horn of the spinal cord, weakness, paralysis and atrophy of the associated skeletal muscles and eventually of the entire trunk, often times causing respiratory failure and early death...
This data repository is not currently reporting usage information. For information on how your repository can submit usage information, please see our documentation.