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Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway
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“For example, in the terminal exon of the TUBA1A gene, weidentified anAgo2cluster overlapping a lissencephaly-causing nonsynonymous mutation, which imparts no obvious detriment to protein function (Tian et al., 2010).”
From Transcriptome-wide Discovery of microRNA Binding Sites in Human Brain (2014) · cites this paper as Tian et al., 2010
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Cited by
Sorted by citations
Transcriptome-wide Discovery of microRNA Binding Sites in Human Brain
Boudreau, R. L., Jiang, P., Gilmore, B. L., Spengler, R. M., Tirabassi, R., Nelson, J. A., Ross, C. A., Xing, Y., & Davidson, B. L. (2014) · Neuron · doi:10.1016/j.neuron.2013.10.062 · Cited by 217
Metadata
- Authors
- Tian, G., Jaglin, X. H., Keays, D. A., Francis, F., Chelly, J., & Cowan, N. J.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-07-05
- Volume
- 19
- Issue
- 18
- Pages
- 3599-3613
- ISSN
- 1460-2083
- 0964-6906
- Cited by
- 71
- References
- 2
- Language
- en
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