Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype-Reference-Cited by-同舟云学术

Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype

Published:2019-11-24 Issue:2 Volume:97 Page:321-328
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Sha Yanwei¹,Wang Xiong²,Yuan JinTing³,Zhu Xingshen⁴,Su Zhiying¹,Zhang Xuequan⁵,Xu Xiaohui⁶,Wei Xiaoli⁴^ORCID

Affiliation:

1. Department of Andrology, United Diagnostic and Research Center for Clinical Genetics, School of Public Health and Women and Children's HospitalXiamen University Xiamen Fujian China

2. Reproductive Medicine CenterAffiliated Yantai Yuhuangding Hospital of Qingdao University Yantai Shandong China

3. School of Environmental Science and EngineeringTianjin University Tianjin China

4. School of Pharmaceutical SciencesXiamen University Xiamen Fujian China

5. Department of AndrologyXiamen Children's Hospital Xiamen Fujian China

6. Laboratory of genetics and cell biology, Medical collegeQingdao University Qingdao Shandong China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13662

Reference33 articles.

1. Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation

2. National, Regional, and Global Trends in Infertility Prevalence Since 1990: A Systematic Analysis of 277 Health Surveys

3. Lack of a head in human spermatozoa from sterile patients: a syndrome associated with impaired fertilization**Supported by grant 0934 from the Consejo Nacional de Investigaciones Científicas y Técnicas.

4. Morphogenesis of the decapitated and decaudated sperm defect in two brothers

5. The Glycosylphosphatidylinositol-Anchored Serine Protease PRSS21 (Testisin) Imparts Murine Epididymal Sperm Cell Maturation and Fertilizing Ability1

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