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J M Griffoin

Showing results (1-10 of 6) with videos related to

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The British Journal of Ophthalmology|March 27, 2001
Retinal dystrophies caused by mutations in RPE65: assessment of visual functionsC P Hamel, J M Griffoin, L Lasquellec, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 geneF Marlhens, J M Griffoin, C Bareil, et al.
Human Genetics|January 26, 2002
Mutation spectrum and splicing variants in the OPA1 geneC Delettre, J M Griffoin, J Kaplan, et al.
Nature Genetics|November 5, 1997
Mutations in RPE65 cause Leber's congenital amaurosisF Marlhens, C Bareil, J M Griffoin, et al.
Journal Francais D'Ophtalmologie|January 5, 2001
[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes]C P Hamel, J M Griffoin, C Bazalgette, et al.
Nature Genetics|October 4, 2000
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyC Delettre, G Lenaers, J M Griffoin, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
The British Journal of Ophthalmology|March 27, 2001
Retinal dystrophies caused by mutations in RPE65: assessment of visual functionsC P Hamel, J M Griffoin, L Lasquellec, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 geneF Marlhens, J M Griffoin, C Bareil, et al.
Human Genetics|January 26, 2002
Mutation spectrum and splicing variants in the OPA1 geneC Delettre, J M Griffoin, J Kaplan, et al.
Nature Genetics|November 5, 1997
Mutations in RPE65 cause Leber's congenital amaurosisF Marlhens, C Bareil, J M Griffoin, et al.
Journal Francais D'Ophtalmologie|January 5, 2001
[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes]C P Hamel, J M Griffoin, C Bazalgette, et al.
Nature Genetics|October 4, 2000
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyC Delettre, G Lenaers, J M Griffoin, et al.
Pageof 1