The essential role of NDE1 in extreme microcephaly

Clinical Genetics

Volumn 80, Issue 3, 2011, Pages 241-242

  Ghannad, M ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

NDE1 PROTEIN; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

CARBOXY TERMINAL SEQUENCE; CELL MIGRATION; CELLULAR DISTRIBUTION; CENTROSOME; EXON; FRAMESHIFT MUTATION; HUMAN; MICROCEPHALY; NERVOUS SYSTEM DEVELOPMENT; NOTE; PRIORITY JOURNAL; PROTEIN LOCALIZATION;

EID: 79961123026     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2011.01753.x     Document Type: Note

References (2)

1. Bakircioglu M, Carvalho OP, Khurshid M et al. The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis. Am J Hum Genet 2011: 88 (5): 523-535.
2. Alkuraya FS, Cai X, Emery C et al. Human mutations in NDE1 cause extreme microcephaly with lissencephaly. Am J Hum Genet 2011: 88 (5): 536-547.