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Human Molecular Genetics|June 6, 2013
The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse modelsRocky G Gogliotti, Herminio Cardona, Jasbir Singh, et al.
American Journal of Human Genetics|May 3, 2011
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]Fowzan S Alkuraya, Xuyu Cai, Carina Emery, et al.
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