Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients - Concepedia

Concepedia

Publication | Open Access

Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Clinical Course and Description of Causal Mutations in Two Patients

DOI Full Paper Access

47

Citations

17

References

2001

Year

Luigi Bouchard, Marie‐France Robert, Dmitriy A. Vinarov, Charles A. Stanley, Geoffrey N. Thompson, Andrew A. M. Morris, James V. Leonard, Patti A. Quant, Betty Y.L. Hsu, Avihu Boneh,

Pediatric Research

Mitochondrial MyopathyClinical CourseMendelian DisorderMitochondrial BiogenesisMitochondrial FunctionGenetic DisorderGeneticsMolecular BiologyPathologyMolecular GeneticsCausal MutationsMedicine

References

	Year	Citations

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