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Article

A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest

19 Feb 2019

Abstract excerpt

STUDY QUESTION: Are there genetic variants that can be used for the clinical evaluation of azoospermic men? SUMMARY ANSWER: A novel homozygous frame-shift mutation in the MEIOB gene was identified in three azoospermic patients from two different families. WHAT IS KNOWN ALREADY: Up to 1% of all men have complete absence of sperm in the semen, a condition known as azoospermia. There are very few tools for...

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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PMID: 30838384
DOI: 10.1093/humrep/dez016

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A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrestPMID 30838384Read ↗

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