Loss‐of‐function mutation in <i>TSGA10</i> causes acephalic spermatozoa phenotype in human
- DOI
- 10.1002/mgg3.1284
- Published
- 2020-05-15
- Container
- Molecular Genetics & Genomic Medicine
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/mgg3.1284,
title = {Loss‐of‐function mutation in <i>TSGA10</i> causes acephalic spermatozoa phenotype in human},
author = {Yuanyuan Ye and Xiaoli Wei and Yanwei Sha and Na Li and Xiaohong Yan and Ling Cheng and Duanrui Qiao and Weidong Zhou and Rongfeng Wu and Qiaobin Liu and Youzhu Li},
year = {2020},
journal = {Molecular Genetics \& Genomic Medicine},
doi = {10.1002/mgg3.1284},
url = {https://doi.org/10.1002/mgg3.1284}
}RIS
TY - JOUR TI - Loss‐of‐function mutation in <i>TSGA10</i> causes acephalic spermatozoa phenotype in human AU - Yuanyuan Ye AU - Xiaoli Wei AU - Yanwei Sha AU - Na Li AU - Xiaohong Yan AU - Ling Cheng AU - Duanrui Qiao AU - Weidong Zhou AU - Rongfeng Wu AU - Qiaobin Liu AU - Youzhu Li PY - 2020 JO - Molecular Genetics & Genomic Medicine DO - 10.1002/mgg3.1284 UR - https://doi.org/10.1002/mgg3.1284 ER -
APA
Ye, Y., Wei, X., Sha, Y., Li, N., Yan, X., Cheng, L., Qiao, D., Zhou, W., Wu, R., Liu, Q., & Li, Y. (2020). Loss‐of‐function mutation in <i>TSGA10</i> causes acephalic spermatozoa phenotype in human. Molecular Genetics & Genomic Medicine. https://doi.org/10.1002/mgg3.1284
Source records
- crossref · retrieved 2026-09-24T21:47:23.148Z