Corinne Mimault

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

Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.

Odile Boespflug‐Tanguy, Corinne Mimault, Judith Melki et al. · PubMed · 1994 · 60 citations

Pelizaeus — Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene

Danielle Pham-Dinh, Odile Boespflug‐Tanguy, Corinne Mimault et al. · Human Molecular Genetics · 1993 · 22 citations

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