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Accession: PRJNA634928 ID: 634928

Empty follicle syndrome caused by non-cleavable mutation of ZP2 furin cleavage site

A rare damaging variant in the CFCS domain of ZP2 was identified by whole-exome sequencing in three unrelated families with clinical manifestations suggestive of GEFS.
AccessionPRJNA634928
Data TypeRaw sequence reads
ScopeMultispecies
Grants
  • "the Science and Technology Major Project of the Ministry of Science and Technology of Hunan Province" (Grant ID 2017SK1032, Ministry of Science and Technology of Hunan Province)
SubmissionRegistration date: 25-May-2020
Reproductive and Genetic Hospital of CITIC-Xiangya
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments8
Other datasets
BioSample8
SRA Data Details
ParameterValue
Data volume, Gbases113
Data volume, Mbytes42716

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