Condition: POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
rs121908462 in
ADGRG1 gene and
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
PMID 22238662 2012 Disease-associated mutations prevent GPR56-collagen III interaction.
PMID 16240336 2005 Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.
PMID 24949629 2014 Mechanism for adhesion G protein-coupled receptor GPR56-mediated RhoA activation induced by collagen III stimulation.
PMID 21723461 2011 A novel GPR56 mutation causes bilateral frontoparietal polymicrogyria.
PMID 15044805 2004 G protein-coupled receptor-dependent development of human frontal cortex.
PMID 21349848 2011 Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms.
PMID 21723461 2011 Here we report a novel missense mutation of GPR56, E496K, identified in a consanguineous pedigree with bilateral frontoparietal polymicrogyria.