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Clinical and molecular features of 40 Chinese patients with idiopathic hypogonadotropic hypogonadism
BACKGROUND: Male idiopathic hypogonadotropic hypogonadism (IHH) is a heterogeneous clinical rare genetic disorder that can be divided into two forms: Kallmann syndrome (KS) and olfactory normal IHH (nIHH). Nearly half of unknown pathogenic genes and related pathogenic mechanisms have yet to be explo...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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AME Publishing Company
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560348/ https://www.ncbi.nlm.nih.gov/pubmed/37814704 http://dx.doi.org/10.21037/tau-23-225 |