Mutation Details for c.3873+23delA
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cDNA Name
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c.3873+23delA
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Exon or Intron
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intron 23
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Legacy Exon or Intron
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intron 20
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4005+23delA
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Other Details
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Contributors
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Angius A., Stasi M., Becchetti T. , Furbetta M.
2008-06-03
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Institute
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Sez. Clinica di Pediatria Medica e Chirurgica, Lab. Genetica Molecolare, Università degli Studi di Perugia, Italy
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Submitted Phenotype Details
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This deletion was detected by DGGE analysis and confirmed by Sequencing in a adult patient with oligospermia undergoing screening due to infertility treatment.
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Reference
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To check if there are any papers published about this mutation/variant on PubMed, please click here.
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