๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

New Therapeutic Approaches to Spinal Muscular Atrophy

โœ Scribed by Aga Lewelt; Tara M. Newcomb; Kathryn J. Swoboda

Book ID
107545886
Publisher
Springer
Year
2011
Tongue
English
Weight
269 KB
Volume
12
Category
Article
ISSN
1528-4042

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Therapeutics development for spinal musc
Therapeutics development for spinal muscular atrophy
โœ Sumner, Charlotte J. ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› American Society for Experimental NeuroTherapeutic ๐ŸŒ English โš– 460 KB

Spinal muscular atrophy is an autosomal recessive motor neuron disease that is the leading inherited cause of infant and early childhood mortality. Spinal muscular atrophy is caused by mutation of the telomeric copy of the survival motor neuron gene (SMN1), but all patients retain a centromeric copy

Invertebrate models of spinal muscular a
Invertebrate models of spinal muscular atrophy: Insights into mechanisms and potential therapeutics
โœ Stuart J. Grice; James N. Sleigh; Ji-Long Liu; David B. Sattelle ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 759 KB

## Abstract Invertebrate genetic models with their tractable neuromuscular systems are effective vehicles for the study of human nerve and muscle disorders. This is exemplified by insights made into spinal muscular atrophy (SMA) using the fruit fly __Drosophila melanogaster__ and the nematode worm