New case of mitochondrial HMG-CoA synthase deficiency. Functional analysis of eight mutations - Concepedia

Concepedia

Publication | Open Access

New case of mitochondrial HMG-CoA synthase deficiency. Functional analysis of eight mutations

DOI Full Paper Access

28

Citations

14

References

2013

Year

Mónica Ramos, Sebastián Menao, María Arnedo, Beatriz Puisac, María Concepción Gil‐Rodríguez, Maria Esperanza Teresa‐Rodrigo, María Hernández-Marcos, Germaine Pierre, Uma Ramaswami, Carolina Baquero‐Montoya,

European Journal of Medical Genetics

Mendelian DisorderMitochondrial BiogenesisBiochemistryMitochondrial FunctionNew CaseGeneticsNatural SciencesMitochondrial DynamicGenetic DisorderDna ReplicationMolecular BiologyMitochondrial MedicineMolecular GeneticsFunctional AnalysisMedicine

References

	Year	Citations

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