Grégory Raux

University of Rouen 
"Grégory Raux"
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Dominique Campion grad student 2002 University of Rouen
 (Bases moléculaires des pathologies mendéliennes et complexes : stratégies d'études moléculaires et avancées technologiques)
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Raux G, Bumsel E, Hecketsweiler B, et al. (2007) Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human Molecular Genetics. 16: 83-91
Lesca G, Burnichon N, Raux G, et al. (2006) Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients. Human Mutation. 27: 598
Rovelet-Lecrux A, Hannequin D, Raux G, et al. (2006) APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nature Genetics. 38: 24-6
Le Ber I, Martinez M, Campion D, et al. (2004) A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. Brain : a Journal of Neurology. 127: 1979-92
Maréchal L, Raux G, Dumanchin C, et al. (2003) Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation American Journal of Medical Genetics - Neuropsychiatric Genetics. 119: 114-117
Jacquet H, Raux G, Thibaut F, et al. (2002) PRODH mutations and hyperprolinemia in a subset of schizophrenic patients Human Molecular Genetics. 11: 2243-2249
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