Associated Papers
A novel frameshift DDHD1 mutation in a patient with hereditary spastic paraplegia type 28: Case report and review of the literature.
Pinheiro RG et al.
Parkinsonism & Related Disorders, 2024
A novel frameshift mutation of DDHD1 in a Japanese patient with autosomal recessive spastic paraplegia.
Miura S et al.
European Journal of Medical Genetics, 2016
A Novel Missense Mutation of the DDHD1 Gene Associated with Juvenile Amyotrophic Lateral Sclerosis.
Wu C et al.
Frontiers in Aging Neuroscience, 2016
Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations.
Liguori R et al.
Journal of Neurology, 2014
Select a paper to view details