A large Turkish pedigree with multiple endocrine neoplasia type 1 syndrome carrying a rare mutation: c.1680_1683 del TGAG

BACKGROUND/AIMS: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome characterized by tumors arising from endocrine glands with no specific genotype-phenotype correlation. Here, we report the largest Turkish kindred with MEN1 syndrome which inherited a scarce MEN1 mutation g...

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Detalhes bibliográficos
Publicado no:Turk J Gastroenterol
Main Authors: Özer Demirtaş, Coşkun, Ata, Pınar, Çetin, Ali, Türkyılmaz, Ayberk, Güney Duman, Deniz
Formato: Artigo
Idioma:Inglês
Publicado em: Turkish Society of Gastroenterology 2020
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7480197/
https://ncbi.nlm.nih.gov/pubmed/32897224
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/tjg.2020.19830
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