Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60 - Concepedia

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Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

DOI Full Paper Access

368

Citations

9

References

2002

Year

Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu‐Rebeix, Costa Georgopoulos, Debbie Ang, Marit N. Nielsen, Claire‐Sophie Davoine, Alexis Brice, Bertrand Fontaine, Niels Gregersen,

The American Journal of Human Genetics

BiologyMitochondrial FunctionGenetic DisorderMedicineGeneticsMolecular GeneticsMitochondrial Chaperonin Hsp60Gene EncodingNeuromuscular Pathology

References

	Year	Citations

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