supplementary file - A heterozygous mutation in CCDC88C gene causes early onset pure hereditary spastic paraplegia
- Resource Type
- Authors
- Yahia, Ashraf; Zhefan Stephen Chen; Ahmed, Ammar E.; Emad, Sara; Rawaa Adil; Rayan Abubaker; Taha, Shaimaa Omer M.A.; Salih, Mustafa A.; Elsayed, Liena; Chan, Ho Yin Edwin; Stevanin, Giovanni
- Source
- Subject
- musculoskeletal diseases
congenital, hereditary, and neonatal diseases and abnormalities
nervous system diseases
- Language
Supplementary material for "A heterozygous mutation in in CCDC88C gene causes early onset pure hereditary spastic paraplegia".