Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system-Reference-Cited by-同舟云学术

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system

Published:2010-12-22 Issue:1 Volume:32 Page:116-125
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Monnot Sophie,Gigarel Nadine,Samuels David C.,Burlet Philippe,Hesters Laetitia,Frydman Nelly,Frydman René,Kerbrat Violaine,Funalot Benoit,Martinovic Jelena,Benachi Alexandra,Feingold Josué,Munnich Arnold,Bonnefont Jean-Paul,Steffann Julie

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21417/fullpdf

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3. Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development;Bouchet;J Med Genet,2006

4. Random genetic drift determines the level of mutant mtDNA in human primary oocytes;Brown;Am J Hum Genet,2001

5. The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells;Cao;Nat Genet,2007

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