Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos

BACKGROUND: TUBB8 is a primate-specific β-tubulin isotype whose expression is confined to oocytes and the early embryo. We previously found that mutations in TUBB8 caused oocyte maturation arrest. The objective was to describe newly discovered mutations in TUBB8 and to characterize the accompanying...

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Pubblicato in:J Med Genet
Autori principali: Feng, Ruizhi, Yan, Zheng, Li, Bin, Yu, Min, Sang, Qing, Tian, Guoling, Xu, Yao, Chen, Biaobang, Qu, Ronggui, Sun, Zhaogui, Sun, Xiaoxi, Jin, Li, He, Lin, Kuang, Yanping, Cowan, Nicholas J., Wang, Lei
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5035199/
https://ncbi.nlm.nih.gov/pubmed/27273344
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2016-103891
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