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Disease Info Card
Cobblestone Lissencephaly
Information about Cobblestone Lissencephaly: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Cobblestone Lissencephaly
Most recent studies have shown that Cobblestone Lissencephaly shares some biological mechanisms with congenital-abnormality, congenital-anomaly-of-brain, congenital-muscular-dystrophy-(disorder), cortical-dysplasia, dysplasia, dystrophy, ectopic-tissue, epilepsy, eye-abnormalities, fukuyama-type-congenital-muscular-dystrophy, hydrocephalus, hypoplasia, lissencephaly, muscle-eye-brain-disease, muscle-hypotonia, muscular-dystrophy, polymicrogyria, walker-warburg-congenital-muscular-dystrophy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cobblestone Lissencephaly, and have been seen in publications frequently: Basement Membrane Assembly, Brain Development, Cell Adhesion, Forebrain Development, Glycosylation, Localization, Membrane Assembly, Myelination, Nervous System Development, Neuroblast Migration, Neurogenesis, Neuron Migration, Pathogenesis, Protein Glycosylation, Secretion, System Development
Quite a number of genes have been found to play important roles in Cobblestone Lissencephaly, such as APBB1, APLP1, APLP2, DAG1, DCX, DMD, FKRP, FKTN, JUN, LMNA, PAFAH1B1, POMGNT1, POMT1, POMT2, PSEN1, PTK2, RELN. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.