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A novel POF1B variant in a Chinese patient is associated with premature ovarian failure
Clinical Genetics ( IF 3.5 ) Pub Date : 2021-08-23 , DOI: 10.1111/cge.14048 Zhuang-Zhuang Yuan 1, 2 , Chen-Yu Wang 2 , Jie-Yuan Jin 2 , Yue Sheng 2 , Mei-Fang Zhao 2 , Liang-Liang Fan 1, 2 , Ai-Qian Zhang 1
A novel mutation of POF1B was identified in a patient with premature ovarian failure.
更新日期：2021-08-23
Clinical Genetics ( IF 3.5 ) Pub Date : 2021-08-23 , DOI: 10.1111/cge.14048 Zhuang-Zhuang Yuan 1, 2 , Chen-Yu Wang 2 , Jie-Yuan Jin 2 , Yue Sheng 2 , Mei-Fang Zhao 2 , Liang-Liang Fan 1, 2 , Ai-Qian Zhang 1
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