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Article

Severe obesity, hypogonadotropic hypogonadism and a WDR11 gene mutation.

QJM : monthly journal of the Association of Physicians - 22 Mar 2022

Lu D, Yang J, Zhang J, Guo X

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Share to Hypogonadism
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Identifiers

PMID: 34741523
DOI: 10.1093/qjmed/hcab279

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 9 Sept 2026.

Related research

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Severe obesity, hypogonadotropic hypogonadism and a WDR11 gene mutation.PMID 34741523Read ↗

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WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.Semantic proximity Read ↗

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A leptin missense mutation associated with hypogonadism and morbid obesity.Semantic proximity Read ↗

Adult-onset reversible idiopathic hypogonadotropic hypogonadism in male adult carrying a WDR11 missense mutation.Semantic proximity Read ↗

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