Ultrastructural changes in diaphragm neuromuscular junctions in a severe mouse model for Spinal Muscular Atrophy and their prevention by bifunctional U7 snRNA correcting SMN2 splicing
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference50 articles.
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2. Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy∗ leads to massive cell death in early mouse embryos;Schrank;Proc Natl Acad Sci USA,1997
3. The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis;Fischer;Cell,1997
4. SMN-mediated assembly of RNPs: a complex story;Meister;Trends Cell Biol,2002
5. The SMN complex, an assemblyosome of ribonucleoproteins;Paushkin;Curr Opin Cell Biol,2002
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