Human genes for lissencephaly
Lissencephaly [DOID:0050453]
A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.
Synonyms: lissencephaly, DOID:0050453, lissencephalies
Linkouts: OMIM #1 #2 #3 #4 #5 #6 #7 #8