Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

scientific article published in August 1990

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0006-291X(90)90490-E
P698PubMed publication ID2390098

P2093author name stringBleeker-Wagemakers EM
Westerveld A
Bolhuis PA
Van den Bogert C
Tabak HF
Van Schooneveld MJ
Ponne NJ
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectmitochondrial DNAQ27075
P304page(s)994-997
P577publication date1990-08-01
P1433published inBiochemical and Biophysical Research CommunicationsQ864228
P1476titleRapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.
P478volume170

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cites work (P2860)
Q70659381A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis
Q34742495A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
Q89293794Advances in methods for reducing mitochondrial DNA disease by replacing or manipulating the mitochondrial genome
Q57721287Chapter 4 Leber's Hereditary Optic Neuropathy
Q33540913Clinical, biochemical and molecular genetic features of Leber's hereditary optic neuropathy
Q40437295Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems
Q48493411Cytochrome Oxidase Inhibition: A Novel Animal Model of Alzheimer's Disease
Q53181028Cytochrome oxidase deficiency in Alzheimer's disease.
Q24676021Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia
Q72231129High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy
Q34187826Human mitochondrial genetics
Q33672801Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder
Q24679168Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation
Q34495453Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside
Q71853045Leber's hereditary optic neuropathy among Japanese
Q33673825Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.
Q72165050Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation
Q33675684Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations
Q37311405Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
Q44259611Mitochondrial DNA analysis in Leber's hereditary optic neuropathy
Q28278762Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas II
Q37970121Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course
Q40697792Mitochondrial encephalomyopathies: clinical and molecular analysis
Q40549895Mitochondrial mutations and human disease
Q43146795Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy
Q38739621Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome.
Q28281746Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants
Q44597965Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy
Q35643475Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation
Q35199431Prenatal diagnosis of mitochondrial DNA8993 T----G disease
Q48055171Region specific mitochondrial gene expression in the human retina
Q28189572Respiratory chain complex I deficiency
Q37299771Retinitis pigmentosa, ataxia, and mental retardation associated with mitochondrial DNA mutation in an Italian family
Q70484976Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification
Q42558990Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.
Q35250357Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes
Q48706853The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
Q72656122The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy
Q70734410The two locus control of Leber hereditary optic neuropathy and a high penetrance in Japanese pedigrees
Q72268660Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy
Q79314462Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy
Q68213792Two-locus mitochondrial and nuclear gene models for mitochondrial disorders
Q37594930X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

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