Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10367
Gene Symbol: MICU1
MICU1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.310 Biomarker CTD_human Here we report mutations of MICU1 in individuals with a disease phenotype characterized by proximal myopathy, learning difficulties and a progressive extrapyramidal movement disorder. 24336167

2014
Entrez Id: 10367
Gene Symbol: MICU1
MICU1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.310 GeneticVariation BEFREE Here we report mutations of MICU1 in individuals with a disease phenotype characterized by proximal myopathy, learning difficulties and a progressive extrapyramidal movement disorder. 24336167

2014