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Spinal Muscular Atrophy and a Model for Survival of Motor Neuron Protein Function in Axonal Ribonucleoprotein Complexes

Spinal muscular atrophy (SMA) is a neurodegenerative disease that results from loss of function of the SMN1 gene, encoding the ubiquitously expressed survival of motor neuron (SMN) protein, a protein best known for its housekeeping role in the SMN–Gemin multiprotein complex involved in spliceosomal...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Rossoll, Wilfried, Bassell, Gary J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2009
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3718852/
https://ncbi.nlm.nih.gov/pubmed/19343312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/400_2009_4
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