[Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human]

Med Sci (Paris). 2014 Dec;30(12):1087-90. doi: 10.1051/medsci/20143012011. Epub 2014 Dec 24.

[Article in French]

Authors

Michel Kielar¹, Françoise Phan Dinh Tuy², Sara Bizzotto², Richard Belvindrah², Alexandre Croquelois¹, Fiona Francis²

Affiliations

¹ Department of clinical neuroscience, Lausanne University Hospital, University of Lausanne, 1011 Lausanne, Suisse - Department of fundamental neuroscience, University of Lausanne, 1005 Lausanne, Suisse.
² Inserm UMR-S 839, 75005 Paris, France - Sorbonne Universités, Université Pierre et Marie Curie, 75005 Paris, France - Institut du Fer à Moulin, 17, rue du Fer à Moulin 75005 Paris, France.

PMID: 25537038
DOI: 10.1051/medsci/20143012011

No abstract available

Publication types

News
Research Support, Non-U.S. Gov't

MeSH terms

Animals
Classical Lissencephalies and Subcortical Band Heterotopias / genetics
Humans
Malformations of Cortical Development / genetics*
Mice
Microtubule-Associated Proteins / genetics*
Mutation*
Neural Stem Cells*

Substances

Eml1 protein, human
Eml1 protein, mouse
Microtubule-Associated Proteins