Citation Tools
PDFNeurological rarities
Ataxia with oculomotor apraxia type 2: an evolving axonal neuropathy
Download to a citation manager
Download the citation for this article by clicking on one of the following citation managers:
- Cite this article as:
- Ataxia with oculomotor apraxia type 2: an evolving axonal neuropathy
Other content recommended for you
- Autosomal recessive cerebellar ataxias: the current state of affairs
- Republished: A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into order
- A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into order
- Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure
- Clinical heterogeneity of recessive ataxia in the Mexican population
- Diagnosis and management of progressive ataxia in adults
- Freidreich's ataxia with retained reflexes: a phenotype and genotype correlation
- Lucina
- The differential diagnosis of Huntington's disease-like syndromes: ‘red flags’ for the clinician
- A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15