Article

Identification of novel mutation in HYAL3 gene of human oligospermia patients by DNA sequencing

2022-11-03

Abstract excerpt

<h4>Background: </h4> Human male infertility has lot of known molecular components having accurately diagnosis such as Y chromosome deletion and monogenic causes. Only 4% of all infertile male are diagnosed with genetic cases while 60–70% of infertile men still remain without accurate diagnosis and are classified as unexplained. Oligospermia is major cause of human male infertility. Its etiology and pathogenesis a...

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Literature Corpus work: 08dabb84-b003-54a2-b155-7df993913c00
DOI: 10.21203/rs.3.rs-2214316/v1

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