17p13.3   GeneReviews   Google   OMIM   PubMed   [Lissencephaly]

Lissencephaly I

*Gene map locus 17p13.3
ILS
LIS1
Lissencephaly sequence, isolated
Lissencephaly, classic
SBH
SCLH
Subcortical band heterotopia
Subcortical laminar heterotopia
[Clinical features: brain malformation; epilepsy; mental retardation]

LIS1-Related Isolated Lissencephaly
LIS1-Related Isolated Lissencephaly
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
Archives of Neurology
Archives of Neurology
Human Molecular Genetics

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene
Type I Lissencephaly
Human Molecular Genetics
Human Molecular Genetics
Indian Pediatrics


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Edited by Aldo Campana, April 19, 2014