Publication | Closed Access
Functional analysis of a mutation in the SLCO1B1 gene (c.1628T>G) identified in a Japanese patient with pravastatin-induced myopathy
36
Citations
20
References
2009
Year
Pravastatin-induced MyopathyEngineeringGenetic DisorderMedicineGeneticsSlco1b1 GenePathologyMolecular GeneticsDisease Gene IdentificationFunctional AnalysisMolecular DiagnosticsVariant InterpretationClinical Genetics
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