Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia
Human 4-hydroxyphenylpyruvate dioxygenase-like (HPDL) is a putative iron-containing non-heme oxygenase of unknown specificity and biological significance. We report 25 families containing 34 individuals with neurological disease associated with biallelic HPDL variants. Phenotypes ranged from juvenil...
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Text |
Language: | English |
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Oxford University Press
2021
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Online Access: | https://pmc.ncbi.nlm.nih.gov/articles/PMC8219359/ https://pubmed.ncbi.nlm.nih.gov/33970200 http://dx.doi.org/10.1093/brain/awab041 |
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