Publication | Closed Access
A novel mutation in the HSPD1 gene in a patient with hereditary spastic paraplegia
52
Citations
9
References
2007
Year
Novel MutationRare DiseasesMendelian DisorderGenetic DisorderMedicineGeneticsPathologyMolecular GeneticsHspd1 GeneDisease Gene IdentificationHereditary Spastic ParaplegiaNeuromuscular Pathology
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