Atıf İçin Kopyala
Demirtaş C. Ö., Ata P., Çetin A., Turkyilmaz A., Duman D.
TURKISH JOURNAL OF GASTROENTEROLOGY, cilt.31, ss.508-514, 2020 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
31
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Basım Tarihi:
2020
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Doi Numarası:
10.5152/tjg.2020.19830
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Dergi Adı:
TURKISH JOURNAL OF GASTROENTEROLOGY
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, MEDLINE, TR DİZİN (ULAKBİM)
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Sayfa Sayıları:
ss.508-514
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Marmara Üniversitesi Adresli:
Evet
Özet
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 gene.