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Heterogeneity of the Clinical Presentation of the MEN1 LRG_509 c.781C>T (p.Leu261Phe) Variant Within a Three-Generation Family

Multiple neuroendocrine neoplasia type 1 (MEN1) is a rare genetic disorder with an autosomal dominant inheritance, predisposing carriers to benign and malignant tumors. The phenotype of MEN1 syndrome varies between patients in terms of tumor localization, age of onset, and clinical aggressiveness, e...

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Detalles Bibliográficos
Autores principales:	Gilis-Januszewska, Aleksandra, Bogusławska, Anna, Hasse-Lazar, Kornelia, Jurecka-Lubieniecka, Beata, Jarząb, Barbara, Sowa-Staszczak, Anna, Opalińska, Marta, Godlewska, Magdalena, Grochowska, Anna, Skalniak, Anna, Hubalewska-Dydejczyk, Alicja
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067145/ https://www.ncbi.nlm.nih.gov/pubmed/33807230 http://dx.doi.org/10.3390/genes12040512

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