Genetic and Epigenetic Analysis in Korean Patients with Multiple Endocrine Neoplasia Type 1

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a familial syndrome characterized by the parathyroid, pancreas and pituitary tumors. Parathyroid tumors are the most common clinical manifestations, occurring in more than 90% of MEN1 patients. Heterozygous germline mutations of the MENIN gen...

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Autores principales: Chung, Yoon Jung, Hwang, Sena, Jeong, Jong Ju, Song, Sun Yong, Kim, Se Hoon, Rhee, Yumie
Formato: Artigo
Lenguaje:Inglês
Publicado: Korean Endocrine Society 2014
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Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4192817/
https://ncbi.nlm.nih.gov/pubmed/25309785
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3803/EnM.2014.29.3.270
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