| Literature DB >> 17761655 |
Christine E Beattie1, Tessa L Carrel, Michelle L McWhorter.
Abstract
Motoneuron diseases cause paralysis and death due to loss of motoneurons that innervate skeletal muscle. Spinal muscular atrophy is a human motoneuron disease that is genetically linked to the survival motor neuron gene (SMN). Although SMN was identified more than a decade ago, it remains unclear how decreased levels of the SMN protein cause spinal muscular atrophy. The use of animal models, however, offers a crucial tool in determining the function of SMN in this disease. In this review, we discuss our efforts to develop a zebrafish model of spinal muscular atrophy.Entities:
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Year: 2007 PMID: 17761655 DOI: 10.1177/0883073807305671
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987