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Publications by Benoît Arveiler
Foetal Onset of EIF2B Related Disorder in Two Siblings: Cerebellar Hypoplasia With Absent Bergmann Glia and Severe Hypomyelination
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
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Sox2 Conditional Mutation in Mouse Causes Ataxic Symptoms, Cerebellar Vermis Hypoplasia, and Postnatal Defects of Bergmann Glia
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Genetic Hypothyroid Mice: Normal Cerebellar Morphology but Altered Glycerol-3-Phosphate Dehydrogenase in Bergmann Glia
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Oculopalatal Tremor and Severe Late-Onset Cerebellar Ataxia
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Correlative Microscopy of Cerebellar Bergmann Glial Cells
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Family Risk and Related Education and Counseling Needs: Perceptions of Adults With Bipolar Disorder and Siblings of Adults With Bipolar Disorder
American Journal of Medical Genetics, Part A
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EP02.16: Case of Hypoplasia Cerebellar Vermis With Dynamic Ventriculomegaly Change
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Novel Homozygous RARS2 Mutation in Two Siblings Without Pontocerebellar Hypoplasia – Further Expansion of the Phenotypic Spectrum
Orphanet Journal of Rare Diseases
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Severe Mycobacterial Infections in Two Pairs of Chinese Siblings With Interleukin-12 Receptor Β1 Deficiency
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Child Health
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