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Therapeutics development for spinal muscular atrophy

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...

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Bibliografski detalji
Glavni autor: Sumner, Charlotte J.
Format: Artigo
Jezik:Inglês
Izdano: Springer-Verlag 2012
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3593434/
https://ncbi.nlm.nih.gov/pubmed/16554261
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nurx.2006.01.010
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