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- W4366536546 abstract "Multiple endocrine neoplasia type 1 (MEN1) is a rare genetic disorder, resulting from MEN1 gene abnormalities, which causes tumors mainly in the endocrine glands. We experienced a sporadic case of MEN1 complicated with papillary thyroid carcinoma (PTC) and found a novel missense mutation in the patient's MEN1 gene. Her older sister, who showed no typical symptom of MEN1, had a history of PTC, suggesting the presence of another genetic factor involved in PTC development. This case suggests the importance of an individual's genetic background in the development of MEN1 complications." @default.
- W4366536546 created "2023-04-22" @default.
- W4366536546 date "2023-01-01" @default.
- W4366536546 modified "2023-09-27" @default.
- W4366536546 title "A Novel Missense MEN1 Mutation in a Sporadic Case of Multiple Endocrine Neoplasia Type 1 Complicated with Papillary Thyroid Carcinoma" @default.
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- W4366536546 doi "https://doi.org/10.31662/jmaj.2022-0187" @default.
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