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B Leo-Kottler

Showing results (11-20 of 18) with videos related to

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German Journal of Ophthalmology|July 1, 1996
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 geneB Leo-Kottler, M Christ-Adler, B Baumann, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 1, 1995
[Correlation between clinical and molecular genetic findings in Leber's optic atrophy]B Leo-Kottler, M Christ-Adler, B Reck, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathyF K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.
Biochemical and Biophysical Research Communications|May 19, 1997
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathyB Wissinger, D Besch, B Baumann, et al.
Human Molecular Genetics|July 7, 2001
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritanceU E Pesch, B Leo-Kottler, S Mayer, et al.
Human Genetics|March 10, 1999
Mapping and genomic characterization of the gene encoding diacylglycerol kinase gamma (DAGK3): assessment of its role in dominant optic atrophy (OPA1)H Stöhr, J Klein, A Gehrig, et al.
Journal of Medical Genetics|February 3, 2009
Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophyN Fuhrmann, M V Alavi, P Bitoun, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
German Journal of Ophthalmology|July 1, 1996
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 geneB Leo-Kottler, M Christ-Adler, B Baumann, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 1, 1995
[Correlation between clinical and molecular genetic findings in Leber's optic atrophy]B Leo-Kottler, M Christ-Adler, B Reck, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathyF K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.
Biochemical and Biophysical Research Communications|May 19, 1997
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathyB Wissinger, D Besch, B Baumann, et al.
Human Molecular Genetics|July 7, 2001
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritanceU E Pesch, B Leo-Kottler, S Mayer, et al.
Human Genetics|March 10, 1999
Mapping and genomic characterization of the gene encoding diacylglycerol kinase gamma (DAGK3): assessment of its role in dominant optic atrophy (OPA1)H Stöhr, J Klein, A Gehrig, et al.
Journal of Medical Genetics|February 3, 2009
Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophyN Fuhrmann, M V Alavi, P Bitoun, et al.
Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.
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