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Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation
by
Xiong Wang;Hai-Rong Jin;Yuan-Qing Cui;Jie Chen;Yan-Wei Sha;Zhen-Li Gao
in
Case studies
/ Deoxyribonucleic acid
/ DNA
/ Hospitals
/ Infertility
/ Laboratories
/ Letter to the Editor
/ Medical research
/ Mutation
/ Parents & parenting
/ Proteins
/ Sperm
/ Spermatogenesis
/ 案例;世界范围;机能障碍;不孕
2018
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Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation
by
Xiong Wang;Hai-Rong Jin;Yuan-Qing Cui;Jie Chen;Yan-Wei Sha;Zhen-Li Gao
in
Case studies
/ Deoxyribonucleic acid
/ DNA
/ Hospitals
/ Infertility
/ Laboratories
/ Letter to the Editor
/ Medical research
/ Mutation
/ Parents & parenting
/ Proteins
/ Sperm
/ Spermatogenesis
/ 案例;世界范围;机能障碍;不孕
2018
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Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation
by
Xiong Wang;Hai-Rong Jin;Yuan-Qing Cui;Jie Chen;Yan-Wei Sha;Zhen-Li Gao
in
Case studies
/ Deoxyribonucleic acid
/ DNA
/ Hospitals
/ Infertility
/ Laboratories
/ Letter to the Editor
/ Medical research
/ Mutation
/ Parents & parenting
/ Proteins
/ Sperm
/ Spermatogenesis
/ 案例;世界范围;机能障碍;不孕
2018
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Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation
Journal Article
Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation
2018
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Overview
Dear Editor, Male infertility, which affects approximately 20 million people worldwide, is commonly caused by spermatogenic dysfunctions, including severe oligozoospermia, cryptozoospermia, and nonobstructive azoospermia, which are largely genetic in origin.
Publisher
Medknow Publications and Media Pvt. Ltd,Medknow Publications & Media Pvt. Ltd,Medknow Publications & Media Pvt Ltd,Wolters Kluwer Medknow Publications
Subject
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