WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells-Reference-Cited by-同舟云学术

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells

Published:2017-09-13 Issue:10 Volume:140 Page:2597-2609
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Cavallin Mara,Rujano Maria A,Bednarek Nathalie,Medina-Cano Daniel,Bernabe Gelot Antoinette,Drunat Severine,Maillard Camille,Garfa-Traore Meriem,Bole Christine,Nitschké Patrick,Beneteau Claire,Besnard Thomas,Cogné Benjamin,Eveillard Marion,Kuster Alice,Poirier Karine,Verloes Alain,Martinovic Jelena,Bidat Laurent,Rio Marlene,Lyonnet Stanislas,Reilly M Louise,Boddaert Nathalie,Jenneson-Liver Melanie,Motte Jacques,Doco-Fenzy Martine,Chelly Jamel,Attie-Bitach Tania,Simons Matias,Cantagrel Vincent,Passemard Sandrine,Baffet Alexandre,Thomas Sophie,Bahi-Buisson Nadia

Funder

Agence Nationale de la Recherche

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/140/10/2597/23003110/awx218.pdf

Reference35 articles.

1. Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected];Am J Hum Genet,2011

2. The wide spectrum of tubulinopathies: what are the key features for the diagnosis?;Brain J Neurol,2014

3. A developmental and genetic classification for malformations of cortical development: update 2012;Brain J Neurol,2012