The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy.

Spinal muscular atrophy (SMA), which is caused by inactivating mutations in the survival motor neuron 1 (SMN1) gene, is characterized by loss of lower motor neurons in the spinal cord. The gene encoding SMN is very highly conserved in evolution, allowing the disease to be modeled in a range of speci...

Ausführliche Beschreibung

Bibliographische Detailangaben
Hauptverfasser: Sleigh, J, Gillingwater, T, Talbot, K
Format: Journal article
Sprache:English
Veröffentlicht: 2011