Article

Association of PFKM Gene Polymorphisms and Susceptibility to Cryptorchidism in a Chinese Han Population

2022-05-20

Abstract excerpt

Cryptorchidism is one of the most common congenital anomalies in newborn boys. There are various risk factors that have been verified to have relationship with cryptorchidism, including exogenous and genetic, but the pathogenesis of cryptorchidism remains unclear. PFKM gene is a critical gene encodes for a regulatory enzyme, which limits the rate in the pathway of glycolysis. In order to investigate the possible a...

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Literature Corpus work: 4213ba60-7d13-5eb8-a3d9-52b253355504
DOI: 10.21203/rs.3.rs-1666056/v1

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