Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1.

HAMAGUCHI K; CONG N D; YANASE T; IKUYAMA S; GOTO K; TAKAYANAGI R; NAWATA H; KUSUDA Y; SAKATA T

Art

J-GLOBAL ID：200902169392960704 Reference number：99A0266554

Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1.

多発性内分泌腫よう症1型の日本人患者におけるMEN1遺伝子の新規の生殖系列突然変異

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Author (9)： , , , , , , , ,
Material：
Volume： 44 Issue： 1 Page： 43-47 Publication year： 1999
JST Material Number： Z0756A ISSN： 1434-5161 Document type： Article
Article type：短報 Country of issue： United Kingdom (GBR) Language： ENGLISH (EN)

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Congenital diseases,deformities in general. , Carcinogenic mechanisms and factors , Genetic variation

Reference (23)：

AGARWAL, SK. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum Mol Genet. 1997, 6, 1169-1175
AOKI, A. Multiple endocrine neoplasia type 1 presented with manicdepressive disorder : a case report with an identified MEN1 gene mutation. Jpn J Clin Oncol. 1997, 27, 419-422
BASSETT, JH. Characterization of mutations in patients with multiple endocrine neoplasia type 1. Am J Hum Genet. 1998, 62, 232-244
BRANDI, ML. Familial multiple endocrine neoplasia type I : a new look at pathophysiology. Endocr Rev. 1987, 8, 391-405
CHAKRABARTI, R. Deletion mapping of endocrine tumors localizes a second tumor suppressor gene on chromosome band 11q13. Genes Chromosomes Cancer. 1998, 22, 130-137

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