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The essential role of NDE1 in extreme microcephaly
Author(s) -
Ghannad M
Publication year - 2011
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2011.01753.x
Subject(s) - microcephaly , lissencephaly , biology , genetics , neurogenesis , gene
The essential role of centrosomal NDE1 in human cerebral neurogenesis Bakircioglu et al. (2011) The American Journal of Human Genetics 88: 523–535 Human mutations in NDE1 cause extreme microcephaly with lissencephaly Alkuraya et al. (2011) The American Journal of Human Genetics 88: 536–547
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