Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating family

PURPOSE: Variations in many genes may lead to the occurrence of oocyte maturation defects. To investigate the genetic basis of oocyte maturation defects, we performed clinical and genetic analysis of a pedigree. METHODS: The proband with oocyte maturation defect-2 receiving ovulation induction thera...

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Detalles Bibliográficos
Autores principales: Xing, Qiong, Wang, Ruyi, Chen, Beili, Li, Lin, Pan, Hong, Li, Tengyan, Ma, Xu, Cao, Yunxia, Wang, Binbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175565/
https://www.ncbi.nlm.nih.gov/pubmed/32316999
http://dx.doi.org/10.1186/s13048-020-00637-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175565/
https://www.ncbi.nlm.nih.gov/pubmed/32316999
http://dx.doi.org/10.1186/s13048-020-00637-4

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