supplementary file - A heterozygous mutation in CCDC88C gene causes early onset pure hereditary spastic paraplegia

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
Publication Year :: 2020
Publisher :: figshare, 2020.
Abstract: Supplementary material for "A heterozygous mutation in in CCDC88C gene causes early onset pure hereditary spastic paraplegia".

Subjects :: musculoskeletal diseases
congenital, hereditary, and neonatal diseases and abnormalities
nervous system diseases

Full Text Access

Tools