CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria - Concepedia

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CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria

DOI Full Paper Access

73

Citations

38

References

2015

Year

Carol Saunders, Laurie D. Smith, Flemming Wibrand, Kirstine Ravn, Peter Bross, Isabelle Thiffault, Mette Christensen, Andrea M. Atherton, Emily Farrow, Neil Miller,

The American Journal of Human Genetics

Clpb Variants AssociatedAutosomal-recessive Mitochondrial DisorderMendelian DisorderOphthalmologyGenetic DisorderMethylglutaconic AciduriaGeneticsLeber Hereditary Optic NeuropathyDegenerative DiseaseNeurologyDisease Gene IdentificationMedicine

References

	Year	Citations

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