Gene: GPAA1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8733
Gene Symbol: GPAA1
GPAA1 		0.020 GeneticVariation disease BEFREE We describe a sporadic case with onset at 53 years of age and a novel VLOFA phenotype mimicking multiple system atrophy (MSA) of cerebellar type associated with minimal GAA1 expansion. 16092110 2005
Entrez Id: 8733
Gene Symbol: GPAA1
GPAA1 		0.020 Biomarker disease BEFREE Our data suggest that central somatosensory pathway involvement in FA is mainly determined by GAA1 expansion size. 10825709 2000