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A Perturbed MicroRNA Expression Pattern Characterizes Embryonic Neural Stem Cells Derived from a Severe Mouse Model of Spinal Muscular Atrophy (SMA)

Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder and the leading genetic cause of death in infants. Despite the disease-causing gene, survival motor neuron (SMN1), encodes a ubiquitous protein, SMN1 deficiency preferentially affects spinal motor neurons (MNs), leaving the basis...

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Bibliografiske detaljer
Main Authors: Andrea Luchetti, Silvia Anna Ciafrè, Michela Murdocca, Arianna Malgieri, Andrea Masotti, Massimo Sanchez, Maria Giulia Farace, Giuseppe Novelli, Federica Sangiuolo
Format: Artigo
Sprog:Inglês
Udgivet: MDPI AG 2015-08-01
Serier:International Journal of Molecular Sciences
Fag:
Online adgang:http://www.mdpi.com/1422-0067/16/8/18312
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