Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men

BACKGROUND: Hypergonadotropic hypogonadism (HH) is characterized by low sex steroid levels and secondarily elevated gonadotropin levels with either congenital or acquired etiology. Genetic factors leading to HH have yet to be fully elucidated. METHODS: Here, we report on genome and transcriptome dat...

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Detalles Bibliográficos
Autores principales: Deng, Xinxian, Fang, He, Pathak, Asha, Zou, Angela M., Neufeld-Kaiser, Whitney, Malouf, Emily A., Failor, Richard A., Hisama, Fuki M., Liu, Yajuan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537572/
https://www.ncbi.nlm.nih.gov/pubmed/33193636
http://dx.doi.org/10.3389/fgene.2020.557341

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537572/
https://www.ncbi.nlm.nih.gov/pubmed/33193636
http://dx.doi.org/10.3389/fgene.2020.557341

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