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1Department of Internal Medicine, Endocrine Research Institute, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
2Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
3Department of Surgery, Yonsei University College of Medicine, Seoul, Korea.
4Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.
Copyright © 2014 Korean Endocrine Society
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
FH, family history; F, female; fs, frameshift mutation; D, daughter; M, male; ns, nonsense mutation; ms, missense mutation; VIP, VIPoma; int, intron; sp, splice site mutation; S, sister.
aMutations are numbered in relation to the MEN1 cDNA reference sequence (GenBank accession number NM_130799.1); bNovel mutation in the present study or previous reports in Korea; cClincial diagnosis of hyperparathyroidism; dStop codon; eDiscordant codon/nucleotide number in the original report.