Publication | Closed Access
A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene
57
Citations
24
References
2000
Year
Genetic AnalysisMendelian DisorderGenetic DisorderGeneticsMolecular BiologyVariable Myopathy AssociatedMolecular GeneticsDisease Gene IdentificationGenomicsR503c MutationMedicine
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