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LHCGR基因突变（Asp578His）致家族性男性性早熟1例临床特点及基因分析
The aim of the study was to provide a descriptive analysis of familial male-limited precocious puberty (FMPP), which is a rare inherited disease caused by heterozygous constitutively activating mutations of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR). The patient was a ten-month...
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| Publicado en: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
中国当代儿科杂志编辑部
2017
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7389323/ https://ncbi.nlm.nih.gov/pubmed/29132462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2017.11.007 |
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