Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans

American Journal of Human Genetics

Volumn 88, Issue 4, 2011, Pages 494-498

  Gigarel, Nadine ^a   Hesters, Laetitia ^b   Samuels, David C ^c   Monnot, Sophie ^a   Burlet, Philippe ^a   Kerbrat, Violaine ^b   Lamazou, Frédéric ^b   Benachi, Alexandra ^b   Frydman, René ^b   Feingold, Josué ^a   Rotig, Agnes ^a   Munnich, Arnold ^a   Bonnefont, Jean Paul ^a   Frydman, Nelly ^b   Steffann, Julie ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^c VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; BLASTOMERE; CELL STRUCTURE; CONCEPTION; EMBRYO; EMBRYO DEVELOPMENT; FEMALE; GAMETOGENESIS; GENE MUTATION; GENETIC SELECTION; HETEROPLASMY; HUMAN; MAJOR CLINICAL STUDY; MEIOSIS; MELAS SYNDROME; MITOCHONDRIAL DNA DISORDER; MUTANT; NUCLEOTIDE SEQUENCE; OOCYTE; POLAR BODY; PRIORITY JOURNAL;

BLASTOMERES; DNA, MITOCHONDRIAL; EMBRYONIC DEVELOPMENT; FEMALE; HUMANS; MALE; MEIOSIS; MELAS SYNDROME; MERRF SYNDROME; MUTATION; OOCYTES; OOGENESIS; PREGNANCY; PREIMPLANTATION DIAGNOSIS;

ANIMALIA;

EID: 79953725719     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.03.010     Document Type: Article

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