Fabrice Cailloux

Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

Fabrice Cailloux, Fernande Gauthier‐Barichard, Corinne Mimault et al. · European Journal of Human Genetics · 2000 · 185 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Brain Development +10

Proteolipoprotein Gene Analysis in 82 Patients with Sporadic Pelizaeus-Merzbacher Disease: Duplications, the Major Cause of the Disease, Originate More Frequently in Male Germ Cells, but Point Mutations Do Not

Corinne Mimault, G Giraud, Virginie Courtois et al. · The American Journal of Human Genetics · 1999 · 131 citations · Full text

Mendelian Disorder, Sporadic Pelizaeus-merzbacher Disease, Proteolipoprotein Gene Analysis +9

<i>PLP1</i>splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations

Marie‐Noëlle Bonnet‐Dupeyron, Patricia Combes, Paola Santander et al. · Human Mutation · 2008 · 24 citations

Genetics, Pathology, Molecular Genetics +20

Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) gene

Corinne Mimault, Fabrice Cailloux, Genevi�ve Giraud et al. · Human Genetics · 1995 · 16 citations

Allelic Variant, Genetics, Human Polymorphism +4