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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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M Kaiser-Kupfer

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Investigative Ophthalmology & Visual Science|May 1, 1996

Glutathione S-transferase M1 genotype and age-related cataracts. Lack of association in an Italian populationG Alberti, M Oguni, M Podgor, et al.

The Journal of Biological Chemistry|February 15, 1992

Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.

American Journal of Human Genetics|September 23, 2000

Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in FinnsG A Mitchell, L C Brody, I Sipila, et al.

Molecular Vision|January 5, 1999

Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin geneG K Klintworth, J R Sommer, G Obrian, et al.

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Search research articles

Showing results (21-30 of 25) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 25 results.

Investigative Ophthalmology & Visual Science|May 1, 1996

Glutathione S-transferase M1 genotype and age-related cataracts. Lack of association in an Italian populationG Alberti, M Oguni, M Podgor, et al.

The Journal of Biological Chemistry|February 15, 1992

Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.

American Journal of Human Genetics|September 23, 2000

Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35X Jiao, F L Munier, F Iwata, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in FinnsG A Mitchell, L C Brody, I Sipila, et al.

Molecular Vision|January 5, 1999

Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin geneG K Klintworth, J R Sommer, G Obrian, et al.

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