Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 767
Gene Symbol: CA8
CA8
0.310 GermlineCausalMutation disease ORPHANET We define the neurological characteristics of familial cases from multiple branches of a large consanguineous family with cerebellar ataxia, mental retardation (MR), and dysequilibrium syndrome type 3 caused by a mutation in the recently cloned CA8 gene. 21812104 2011
Entrez Id: 767
Gene Symbol: CA8
CA8
0.310 GeneticVariation disease BEFREE We define the neurological characteristics of familial cases from multiple branches of a large consanguineous family with cerebellar ataxia, mental retardation (MR), and dysequilibrium syndrome type 3 caused by a mutation in the recently cloned CA8 gene. 21812104 2011