Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans-Reference-Cited by-同舟云学术

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

Published:2002-10-15 Issue:3 Volume:32 Page:359-369
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kitamura Kunio,Yanazawa Masako,Sugiyama Noriyuki,Miura Hirohito,Iizuka-Kogo Akiko,Kusaka Masatomo,Omichi Kayo,Suzuki Rika,Kato-Fukui Yuko,Kamiirisa Kyoko,Matsuo Mina,Kamijo Shin-ichi,Kasahara Megumi,Yoshioka Hidefumi,Ogata Tsutomu,Fukuda Takayuki,Kondo Ikuko,Kato Mitsuhiro,Dobyns William B.,Yokoyama Minesuke,Morohashi Ken-ichirou

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1009z.pdf

Reference46 articles.

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3. Lambert de Rouvroit, C. & Goffinet, A.M. Neuronal migration. Mech. Dev. 105, 47–56 (2001).

4. Reiner, O. et al. Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit–like repeats. Nature 364, 717–721 (1993).

5. des Portes, V. et al. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heteropia and lissencephaly syndrome. Cell 92, 51–61 (1998).

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