mtDNA heteroplasmy in Leber hereditary optic neuroretinopathy. 1991

V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich

UI MeSH Term Description Entries
D008297 Male Males
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D011995 Recombination, Genetic Production of new arrangements of DNA by various mechanisms such as assortment and segregation, CROSSING OVER; GENE CONVERSION; GENETIC TRANSFORMATION; GENETIC CONJUGATION; GENETIC TRANSDUCTION; or mixed infection of viruses. Genetic Recombination,Recombination,Genetic Recombinations,Recombinations,Recombinations, Genetic
D004272 DNA, Mitochondrial Double-stranded DNA of MITOCHONDRIA. In eukaryotes, the mitochondrial GENOME is circular and codes for ribosomal RNAs, transfer RNAs, and about 10 proteins. Mitochondrial DNA,mtDNA
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D015418 Optic Atrophies, Hereditary Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER). Hereditary Optic Atrophy,Optic Atrophy, Hereditary,Atrophies, Hereditary Optic,Atrophy, Hereditary Optic,Hereditary Optic Atrophies

Related Publications

V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
June 1991, American journal of human genetics,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
January 1997, European journal of human genetics : EJHG,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
July 1992, Biochimica et biophysica acta,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
July 1994, American journal of human genetics,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
September 1991, American journal of human genetics,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
January 1994, Human mutation,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
December 2012, Proceedings of the National Academy of Sciences of the United States of America,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
January 2017, Handbook of experimental pharmacology,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
August 1989, American journal of human genetics,
V Cormier, and A Rötig, and C Geny, and P Cesaro, and J L Dufier, and A Munnich
January 1992, American journal of medical genetics,
Copied contents to your clipboard!