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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Turk J Gastroenterol
Prif Awduron: Özer Demirtaş, Coşkun, Ata, Pınar, Çetin, Ali, Türkyılmaz, Ayberk, Güney Duman, Deniz
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Turkish Society of Gastroenterology 2020
Pynciau:
Original Article
Mynediad Ar-lein: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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