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Results: 1-8 |
Results: 8
TISSUE DISTRIBUTION OF THE ND4 11778 MUTATION IN HETEROPLASMIC LINEAGES WITH LEBER HEREDITARY OPTIC NEUROPATHY/
Authors: JUVONEN V NIKOSKELAINEN E LAMMINEN T PENTTINEN M AULA P SAVONTAUS ML
Citation: V. Juvonen et al., TISSUE DISTRIBUTION OF THE ND4 11778 MUTATION IN HETEROPLASMIC LINEAGES WITH LEBER HEREDITARY OPTIC NEUROPATHY/, Human mutation, 9(5), 1997, pp. 412-417
MTDNA HAPLOTYPE ANALYSIS IN FINNISH FAMILIES WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY
Authors: LAMMINEN T HUOPONEN K SISTONEN P JUVONEN V LAHERMO P AULA P NIKOSKELAINEN E SAVONTAUS ML
Citation: T. Lamminen et al., MTDNA HAPLOTYPE ANALYSIS IN FINNISH FAMILIES WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY, European journal of human genetics, 5(5), 1997, pp. 271-279
MUTATIONS IN SUBUNIT-6 OF THE F1F0-ATP SYNTHASE CAUSE 2 ENTIRELY DIFFERENT DISEASES
Authors: MAJANDER A LAMMINEN T JUVONEN V AULA P NIKOSKELAINEN E SAVONTAUS ML WIKSTROM M
Citation: A. Majander et al., MUTATIONS IN SUBUNIT-6 OF THE F1F0-ATP SYNTHASE CAUSE 2 ENTIRELY DIFFERENT DISEASES, FEBS letters, 412(2), 1997, pp. 351-354
OPHTHALMOLOGIC FINDINGS IN LEBER HEREDITARY OPTIC NEUROPATHY, WITH SPECIAL REFERENCE TO MTDNA MUTATIONS
Authors: NIKOSKELAINEN EK HUOPONEN K JUVONEN V LAMMINEN T NUMMELIN K SAVONTAUS ML
Citation: Ek. Nikoskelainen et al., OPHTHALMOLOGIC FINDINGS IN LEBER HEREDITARY OPTIC NEUROPATHY, WITH SPECIAL REFERENCE TO MTDNA MUTATIONS, Ophthalmology, 103(3), 1996, pp. 504-514
LEBERS PLUS - NEUROLOGICAL ABNORMALITIES IN PATIENTS WITH LEBERS HEREDITARY OPTIC NEUROPATHY
Authors: NIKOSKELAINEN EK MARTTILA RJ HUOPONEN K JUVONEN V LAMMINEN T SONNINEN P SAVONTAUS ML
Citation: Ek. Nikoskelainen et al., LEBERS PLUS - NEUROLOGICAL ABNORMALITIES IN PATIENTS WITH LEBERS HEREDITARY OPTIC NEUROPATHY, Journal of Neurology, Neurosurgery and Psychiatry, 59(2), 1995, pp. 160-164
A MITOCHONDRIAL MUTATION AT NT-9101 IN THE ATP SYNTHASE-6 GENE ASSOCIATED WITH DEFICIENT OXIDATIVE-PHOSPHORYLATION IN A FAMILY WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY
Authors: LAMMINEN T MAJANDER A JUVONEN V WIKSTROM M AULA P NIKOSKELAINEN E SAVONTAUS ML
Citation: T. Lamminen et al., A MITOCHONDRIAL MUTATION AT NT-9101 IN THE ATP SYNTHASE-6 GENE ASSOCIATED WITH DEFICIENT OXIDATIVE-PHOSPHORYLATION IN A FAMILY WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY, American journal of human genetics, 56(5), 1995, pp. 1238-1240
TYPICAL AND ATYPICAL FINDINGS IN LEBER HEREDITARY OPTIC NEUROPATHY
Authors: NIKOSKELAINEN EK HUOPONEN K JUVONEN V LAMMINEN T SAVONTAUS ML
Citation: Ek. Nikoskelainen et al., TYPICAL AND ATYPICAL FINDINGS IN LEBER HEREDITARY OPTIC NEUROPATHY, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1984-1984
THE SPECTRUM OF MITOCHONDRIAL-DNA MUTATIONS IN FAMILIES WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY
Authors: HUOPONEN K LAMMINEN T JUVONEN V AULA P NIKOSKELAINEN E SAVONTAUS ML
Citation: K. Huoponen et al., THE SPECTRUM OF MITOCHONDRIAL-DNA MUTATIONS IN FAMILIES WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY, Human genetics, 92(4), 1993, pp. 379-384
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