14-3-3ε is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller–Dieker syndrome

Author:

Toyo-oka Kazuhito,Shionoya Aki,Gambello Michael J,Cardoso Carlos,Leventer Richard,Ward Heather L,Ayala Ramses,Tsai Li-Huei,Dobyns William,Ledbetter David,Hirotsune Shinji,Wynshaw-Boris Anthony

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference50 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. Assoc. 270, 2838–2842 (1993).

2. Dobyns, W.B., Curry, C.J., Hoyme, H.E., Turlington, L. & Ledbetter, D.H. Clinical and molecular diagnosis of Miller–Dieker syndrome. Am. J. Hum. Genet. 48, 584–594 (1991).

3. Dobyns, W.B., Elias, E.R., Newlin, A.C., Pagon, R.A. & Ledbetter, D.H. Causal heterogeneity in isolated lissencephaly. Neurology 42, 1375–1388 (1992).

4. Ledbetter, S.A., Kuwano, A., Dobyns, W.B. & Ledbetter, D.H. Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly. Am. J. Hum. Genet. 50, 182–189 (1992).

5. 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).

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