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Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

Crossref DOI link: https://doi.org/10.1038/gim.2017.130

Published Print: 2019-05

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Tan, Yue-Qiu

Tu, Chaofeng

Meng, Lanlan

Yuan, Shimin

Sjaarda, Calvin

Luo, Aixiang

Du, Juan

Li, Wen

Gong, Fei

Zhong, Changgao

Deng, Han-Xiang

Lu, Guangxiu

Liang, Ping

Lin, Ge
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Text and Data Mining valid from 2019-05-01

Text and Data Mining valid from 2019-05-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2017.130

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics