Novel bi‐allelic <scp> <i>HPDL</i> </scp> variants cause hereditary spastic paraplegia in a Chinese patient
Hao Yu, Qiao Wei, Wen‐Jiao Luo, Zhi‐Ying Wu
Abstract
The peer review history for this article is available at https://publons.com/publon/10.1111/cge.14056. Data supporting the findings described in this study are available upon request.
Topics & Concepts
Hereditary spastic paraplegiaAlleleGeneticsMedicineParaplegiaBiologyGenePsychiatryPhenotypeSpinal cordHereditary Neurological DisordersNeurological diseases and metabolismLysosomal Storage Disorders Research