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Тяжелые костные осложнения первичного гиперпаратиреоза у молодого пациента с верифицированной мутацией в гене <i>MEN1</i>
Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine tumors. Unfortunately, none of the described MEN1 mutations has been associated with a peculiar clinical phenotype, even within members of the sa...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Endocrinology Research Centre
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761876/ https://www.ncbi.nlm.nih.gov/pubmed/35262299 http://dx.doi.org/10.14341/probl12864 |