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The Spectrum of Common Mutations in CFTR, AR Gene, and the Y Chromosome Microdeletions and Karyotyping Abnormalities in Phenotypic Male with Very Severe Oligozoospermia

2021-05-17

Abstract excerpt

<title>Abstract</title> <p>Male infertility due to very severe oligozoospermia has been associated with a number of genetic risk factors.This association in patients with sperm concentration lower than 1× 10<sup>6</sup> ml are not yet fully studied.The present study aims to investigate the distribution of the mutations in the<italic> CFTR</italic> gene, the CAG repeat expansion of the <italic>AR</italic> gene as...

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Literature Corpus work
2c5c8cc3-9d96-570b-950e-40665b4fb7ba
DOI
10.21203/rs.3.rs-482507/v1
Open publication

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The Spectrum of Common Mutations in CFTR, AR Gene, and the Y Chromosome Microdeletions and Karyotyping Abnormalities in Phenotypic Male with Very Severe OligozoospermiaDOI 10.21203/rs.3.rs-482507/v1
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