New insights into HPDL protein: identification of a novel Bi-allelic variant, docking simulation study, and literature review
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Background: Hereditary Spastic Paraplegia (HSP) is a rare neurodegenerative disorder causing progressive weakness and spasticity in the lower limbs. variants in the HPDL gene are linked to Spastic Paraplegia 83 (SPG83), an autoso... ...
