Transmission of the human mitochondrial genome

Human Reproduction

Volumn 15, Issue SUPPL. 2, 2000, Pages 235-245

  Howell, Neil ^a   Chinnery, P F ^b   Ghosh, S S ^c   Fahy, E ^c   Turnbull, D M ^b   Jansen, Robert ^d  

^a University of Texas Medical Branch School of Medicine   (United States)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

^c Migenix Inc   (United States)

^d NONE

Author keywords

Mitochondrial bottleneck; Mitochondrial disease; Mitochondrial DNA; mtDNA heteroplasmy; mtDNA mutations

Indexed keywords

MITOCHONDRIAL DNA;

ALLELE; CELL STRUCTURE; CONFERENCE PAPER; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA SEQUENCE; EMBRYO DEVELOPMENT; ENCEPHALOMYOPATHY; GENE FREQUENCY; GENE MUTATION; GENE SEGREGATION; GENETIC ANALYSIS; GENETIC DRIFT; GENETIC POLYMORPHISM; HEREDITARY OPTIC ATROPHY; HUMAN; INHERITANCE; LEUKOCYTE; LONGITUDINAL STUDY; MOLECULAR GENETICS; MUTATION RATE; MYOCLONUS EPILEPSY; NONHUMAN; OOCYTE DEVELOPMENT; POINT MUTATION;

FALLOPIA;

EID: 0033646619     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/15.suppl_2.235     Document Type: Conference Paper

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