Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome

PURPOSE: To screen novel mutations in LHCGR responsible for empty follicle syndrome and explore the pathological mechanism of mutations. METHODS: Four affected individuals diagnosed with infertility-associated anovulation or oligo-ovulation from three independent families were recruited. Sanger sequ...

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Veröffentlicht in:J Assist Reprod Genet
Hauptverfasser: Zhang, Zhihua, Wu, Ling, Diao, Feiyang, Chen, Biaobang, Fu, Jing, Mao, Xiaoyan, Yan, Zheng, Li, Bin, Mu, Jian, Zhou, Zhou, Wang, Wenjing, Zhao, Lin, Dong, Jie, Zeng, Yang, Du, Jing, Kuang, Yanping, Sun, Xiaoxi, He, Lin, Sang, Qing, Wang, Lei
Format: Artigo
Sprache:Inglês
Veröffentlicht: Springer US 2020
Schlagworte:
Genetics
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7642116/
https://ncbi.nlm.nih.gov/pubmed/32860205
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-020-01931-2
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