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Publications by Philippe Isope
Cerebellar Ataxia and Coenzyme Q Deficiency Through Loss of Unorthodox Kinase Activity
Molecular Cell
Cell Biology
Molecular Biology
26th Annual Computational Neuroscience Meeting (CNS*2017): Part 2
BMC Neuroscience
Neuroscience
Cellular
Molecular Neuroscience
Related publications
Autosomal Recessive Cerebellar Ataxia Due to STUB1 Deficiency
Clinical Syndromes Associated With Coenzyme Q 10 Deficiency
Essays in Biochemistry
Biochemistry
Molecular Biology
Muscle Coenzyme Q Deficiency in Familial Mitochondrial Encephalomyopathy.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency
Cerebellar Ataxia, Cayman Type
Acute Cerebellar Ataxia and Infectious Mononucleosis.
Postgraduate Medical Journal
Medicine
Myoclonus-Cerebellar Ataxia-Deafness Syndrome
Cerebellar Ataxia-Ectodermal Dysplasia Syndrome
Brachydactyly-Nystagmus-Cerebellar Ataxia Syndrome
