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Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) neuroendocrine tumors (NETs). MEN1 is usually consequent to different germline and somatic mutations of the MEN1 tumor suppress...
שמור ב:
| הוצא לאור ב: | Front Endocrinol (Lausanne) |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Frontiers Media S.A.
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7708377/ https://ncbi.nlm.nih.gov/pubmed/33312161 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.591501 |
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