Gene: MYH6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4624
Gene Symbol: MYH6
MYH6 		0.010 GeneticVariation disease BEFREE We here report on a human myopathy associated with a mutation in a fast myosin heavy chain (MyHC) gene, and also the genetic defect in a hereditary inclusion body myopathy. 11114175 2000