Article

Deletion of <i>FUNDC2</i> and <i>CMC4</i> on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men

2020-03-23

Abstract excerpt

<h4>Background</h4> 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. <h4>Methods</h4> Here, we report on genome and transcriptome data analyses from a male patient with HH and history of growth delay who has an inherited deletion of...

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Literature Corpus work: 9318375b-31a9-5059-b359-b27549a86308
DOI: 10.1101/2020.03.23.004424

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Deletion of <i>FUNDC2</i> and <i>CMC4</i> on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in menDOI 10.1101/2020.03.23.004424Read

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