Bibliography

Mutations in KCND3 cause spinocerebellar ataxia type 22

Mutations in KCND3 cause spinocerebellar ataxia type 22

Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12

Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy

Spatacsin and spastizin act in the same pathway required for proper spinal motor neuron axon outgrowth in zebrafish

Spatacsin and spastizin act in the same pathway required for proper spinal motor neuron axon outgrowth in zebrafish

Autosomal Dominant Spastic ParaplegiasA Review of 89 Families Resulting From a Portuguese Survey

Autosomal Dominant Spastic Paraplegias – A Review of 89 Families Resulting From a Portuguese Survey

Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia

Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia

Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases

Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice

Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice

New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together