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

2020-03-25

Abstract excerpt

<title>Abstract</title> <p>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. <h4>Methods:</h4> The proband with oocyte maturation defect-2 receiving ovulation induction therapy and her parents were selected for clinical detection, whole exome sequencing...

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Literature Corpus work
d2cb37da-5dc6-5caf-9569-3717fd72f551
DOI
10.21203/rs.2.22739/v2
Open publication

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Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating familyDOI 10.21203/rs.2.22739/v2
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