Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease

Mitochondrial DNA (mtDNA) mutations are a common cause of genetic disease with pathogenic mtDNA mutations being detected in approximately 1 in 250 live births1-3 and at least 1 in 10,000 adults in the UK affected by mtDNA disease4. Treatment options for patients with mtDNA disease are extremely limi...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Craven, Lyndsey, Tuppen, Helen A, Greggains, Gareth D, Harbottle, Stephen J, Murphy, Julie L, Cree, Lynsey M, Murdoch, Alison P, Chinnery, Patrick F, Taylor, Robert W, Lightowlers, Robert N, Herbert, Mary, Turnbull, Douglass M
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2010
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2875160/
https://ncbi.nlm.nih.gov/pubmed/20393463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature08958
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