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Publications by Maria do Céu Moreira
Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity
American Journal of Human Genetics
Genetics
Recessive Ataxia With Ocular Apraxia
Archives of Neurology
Related publications
Ataxia-Oculomotor Apraxia Type 1
Erratum To: Ataxia With Oculomotor Apraxia Type 1 Without Oculomotor Apraxia: A Case Report
Journal of Clinical Neurology (Korea
Neurology
Ataxia With Oculomotor Apraxia Type 1 - New Mutation, Characteristic Phenotype
Movement Disorders Clinical Practice
Neurology
Mutation of Senataxin Alters Disease-Specific Transcriptional Networks in Patients With Ataxia With Oculomotor Apraxia Type 2
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Homozygosity Mapping of Spinocerebellar Ataxia With Cerebellar Atrophy and Peripheral Neuropathy to 9q33–34, and With Hearing Impairment and Optic Atrophy to 6p21–23
European Journal of Human Genetics
Genetics
Oculomotor and Vestibular Findings in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Canadian Journal of Neurological Sciences
Medicine
Neurology
Variant Forms of Ataxia Telangiectasia.
Journal of Medical Genetics
Genetics
Genetic Evidence of Heterogeneity in Intrahepatic Cholestasis of Pregnancy
Gut
Gastroenterology
