Author:
Faulkner Nicole E.,Dujardin Denis L.,Tai Chin-Yin,Vaughan Kevin T.,O'Connell Christopher B.,Wang Yu-li,Vallee Richard B.
Publisher
Springer Science and Business Media LLC
Reference49 articles.
1. Dobyns, W. B., Reiner, O., Carrozzo, R. & Ledbetter, D. H. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. J. Am. Med. Soc. 270, 2838–2842 (1993).
2. Reiner, O. et al. Isolation of a Miller–Dieker lissencephaly gene containing G protein β-subunit-like repeats. Nature 364, 717–721 (1993).
3. Lo Nigro, C. et al. Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller–Dieker syndrome. Hum. Mol. Genet. 6, 157–164 (1997).
4. Chong, S. S. et al. A revision of the lissencephaly and Miller–Dieker syndrome critical regions in chromosome 17p13.3. Hum. Mol. Genet. 6, 147–155 (1997).
5. Mizuguchi, M., Takashima, S., Kakita, A., Yamada, M. & Ikeda, K. Lissencephaly gene product. Localization in the central nervous system and loss of immunoreactivity in Miller–Dieker syndrome. Am. J. Pathol. 147, 1142–1151 (1995).
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