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- Q4907578 subject Q7031586.
- Q4907578 abstract "Bilateral frontoparietal polymicrogyria (BFPP) is a genetic disorder with autosomal recessive inheritance that causes a cortical malformation. Our brain has folds in the cortex to increase surface area called gyri and patients with polymicrogyri have an increase number of folds and smaller folds than usual. Polymicrogyria is defined as a cerebral malformation of cortical development in which the normal gyral pattern of the surface of the brain is replaced by an excessive number of small, fused gyri separated by shallow sulci and abnormal cortical lamination. From ongoing research, mutation in GPR56,a member of the adhesion G protein-coupled receptor (GPCR) family, results in BFPP. These mutations are located in different regions of the protein without any evidence of a relationship between the position of the mutation and phenotypic severity. It is also found that GPR56 plays a role in cortical pattering.".
- Q4907578 omim "606854".
- Q4907578 thumbnail GPCR_classification.svg?width=300.
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- Q4907578 wikiPageWikiLink Q7031586.
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- Q4907578 wikiPageWikiLink Q75839.
- Q4907578 wikiPageWikiLink Q785893.
- Q4907578 wikiPageWikiLink Q79927.
- Q4907578 name "Bilateral frontalparietal polymicrogyria".
- Q4907578 omim "606854".
- Q4907578 type Disease.
- Q4907578 type Thing.
- Q4907578 type Q12136.
- Q4907578 comment "Bilateral frontoparietal polymicrogyria (BFPP) is a genetic disorder with autosomal recessive inheritance that causes a cortical malformation. Our brain has folds in the cortex to increase surface area called gyri and patients with polymicrogyri have an increase number of folds and smaller folds than usual.".
- Q4907578 label "Bilateral frontoparietal polymicrogyria".
- Q4907578 depiction GPCR_classification.svg.
- Q4907578 name "Bilateral frontalparietal polymicrogyria".