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pro vyhledávání: '"Daniela Pletto"'
Autor:
Daniela Pletto, Silvia Capra, Adele Finardi, Francesca Colciaghi, Paola Nobili, Giorgio Stefano Battaglia, Denise Locatelli, Cinzia Cagnoli
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0199105 (2018)
Spinal Muscular Atrophy (SMA) is a severe autosomal recessive disease characterized by selective motor neuron degeneration, caused by disruptions of the Survival of Motor Neuron 1 (Smn1) gene. The main product of SMN1 is the full-length SMN protein (
Externí odkaz:
https://doaj.org/article/da9d6add2f674cbe9eeca9ceb75941bc
