Jean‐Michel Griffoin

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

Cécile Delettre, Guy Lenaers, Jean‐Michel Griffoin et al. · Nature Genetics · 2000 · 1.4K citations

Neurodegenerative Diseases, Mitochondrial Function, Ophthalmology +9

Mutation spectrum and splicing variants in the OPA1 gene

Cécile Delettre, Jean‐Michel Griffoin, Josseline Kaplan et al. · Human Genetics · 2001 · 379 citations

Somatic Variant, Genetics, Molecular Genetics +5

Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene

F. Marlhens, Jean‐Michel Griffoin, Corinne Bareil et al. · European Journal of Human Genetics · 1998 · 62 citations · Full text

Ocular Disease, Rpe65 Gene, Retina +8

[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].

Ch. P. Hamel, Jean‐Michel Griffoin, Ch. Bazalgette et al. · Journal Français d Ophtalmologie · 2000 · 28 citations

Novel Mutations in<i>MYO7A</i>and<i>USH2A</i>in Usher Syndrome

C. Maubaret, Jean‐Michel Griffoin, Bernard Arnaud et al. · Ophthalmic Genetics · 2005 · 18 citations