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Publications by Adnan Y Manzur
Mutations in XRCC1 Cause Cerebellar Ataxia and Peripheral Neuropathy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Related publications
SETX Mutations Are a Frequent Genetic Cause of Juvenile and Adult Onset Cerebellar Ataxia With Neuropathy and Elevated Serum Alpha-Fetoprotein
Orphanet Journal of Rare Diseases
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Pharmacology
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
American Journal of Human Genetics
Genetics
Bi-Allelic ADPRHL2 Mutations Cause Neurodegeneration With Developmental Delay, Ataxia, and Axonal Neuropathy
American Journal of Human Genetics
Genetics
Brain Hypometabolism in Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome
Research in Vestibular Science
Cerebellar Ataxia With Neuropathy and Bilateral Vestibular Areflexia Syndrome
Otology and Neurotology
Medicine
Otorhinolaryngology
Sensory Systems
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Ataxia, Peripheral Neuropathy, and Anti-Gliadin Antibody. Guilt by Association?
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Periaxin Mutations Cause Recessive Dejerine-Sottas Neuropathy
American Journal of Human Genetics
Genetics
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
Mutations in KARS Cause a Severe Neurological and Neurosensory Disease With Optic Neuropathy
Human Mutation
Genetics
