Lissencephaly with marked ventricular dilation, agenesis of corpus callosum, and cerebellar hypoplasia caused by TUBA1A mutation-Reference-Cited by-同舟云学术

Lissencephaly with marked ventricular dilation, agenesis of corpus callosum, and cerebellar hypoplasia caused by TUBA1A mutation

Published:2013-03 Issue:3 Volume:35 Page:274-279
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Okumura Akihisa,Hayashi Masaharu,Tsurui Hiromichi,Yamakawa Yoko,Abe Shinpei,Kudo Takahiro,Suzuki Ryuyo,Shimizu Toshiaki,Shimojima Keiko,Yamamoto Toshiyuki

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference13 articles.

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2. Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A);Poirier;Hum Mutat,2007

3. Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A;Fallet-Bianco;Brain,2008

4. Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype;Lecourtois;Acta Neuropathol,2010

5. Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations;Bahi-Buisson;J Med Genet,2008

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