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Laurent Cavalier

Centre national de la recherche scientifique

4

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The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

2000 Nature Genetics
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Clinical Nosologic and Genetic Aspects of Joubert and Related Syndromes

1999 Journal of Child Neurology
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Ataxia with Isolated Vitamin E Deficiency: Heterogeneity of Mutations and Phenotypic Variability in a Large Number of Families

1998 American Journal of Human Genetics
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Giant axonal neuropathy: clinical study and genetic mapping

1997 Neuromuscular Disorders
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