异质性
卵裂球
植入前遗传学诊断
生物
线粒体DNA
遗传学
突变
胚胎
突变率
粒线体疾病
胚胎发生
基因
作者
Suzanne C.E.H. Sallevelt,J. Dreesen,Edith Coonen,Aimée Paulussen,Debby M.E.I. Hellebrekers,Christine de Die‐Smulders,Hubert J.M. Smeets,Patrick Lindsey
标识
DOI:10.1136/jmedgenet-2017-104633
摘要
Our findings support a single-blastomere biopsy PGD protocol for the m.3243A>G mutation as the diagnostic error rate is very low. As in the early preimplantation embryo no mtDNA replication seems to occur and the mtDNA is divided randomly among the daughter cells, we conclude this result to be independent of the specific mutation and therefore applicable to all mtDNA mutations.
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