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The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models.

Heather L. Plasterer, C. Heier, C. DiDonato, 2013, Human molecular genetics.

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].

C. Walsh, G. Gascon, F. Alkuraya, 2011, American journal of human genetics.

Electrophysiological changes in hippocampal slices isolated from rats embedded with depleted uranium fragments.

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Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].

G. Gascon, F. Alkuraya, R. Hill, 2011, American journal of human genetics.

The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models.

Heather L. Plasterer, C. Heier, C. DiDonato, 2013, Human molecular genetics.