Hereditary spastic paraplegia: Clues from a rare disorder for a common problem?
IUBMB Life
Saved in:
Main Authors: | Burgunder, J.-M., Hunziker, W. |
---|---|
Other Authors: | MEDICINE |
Format: | Review |
Published: |
2014
|
Subjects: | |
Online Access: | http://scholarbank.nus.edu.sg/handle/10635/118065 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
Hereditary spastic paraplegia: Clues from a rare disorder for a common problem?
by: Burgunder, J.-M., et al.
Published: (2016) -
Expanding the DARS phenotype: late-adult onset myelopathy and leukoencephalopathy
by: Tan, Ai Huey, et al.
Published: (2023) -
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis
by: Ahmed, Mustafa Y, et al.
Published: (2020) -
Inner retinal dysfunction in the autosomal recessive spastic ataxia of Charlevoix-Saguenay
by: Borruat, F.-X, et al.
Published: (2020) -
On QF-3 Rings and Hereditary Rings
by: Maliwan Tunapan
Published: (2023)