A Novel Von Hippel-Lindau case with germline mutation at codon 167 (CGG to TGG) having endocrine microadenomatosis of the pancreas

Tomotaka Akatsu, Koichi Aiura, Yasuhiro Ito, Masakazu Ueda, Kaori Kameyama, Masaki Kitajima

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)3145-3148
Number of pages4
JournalDigestive Diseases and Sciences
Volume52
Issue number11
DOIs
Publication statusPublished - 2007 Nov

Fingerprint

Islet Cell Adenoma
von Hippel-Lindau Disease
Multiple Endocrine Neoplasia Type 1
X Ray Computed Tomography
Germ-Line Mutation
Pancreatic Neoplasms
Islets of Langerhans
Codon
Pancreas
Differential Diagnosis

Keywords

  • Clear cell
  • Endocrine tumor
  • Germline mutation
  • Microadenomatosis
  • Pancreas
  • Von Hippel-Lindau

ASJC Scopus subject areas

  • Gastroenterology

Cite this

A Novel Von Hippel-Lindau case with germline mutation at codon 167 (CGG to TGG) having endocrine microadenomatosis of the pancreas. / Akatsu, Tomotaka; Aiura, Koichi; Ito, Yasuhiro; Ueda, Masakazu; Kameyama, Kaori; Kitajima, Masaki.

In: Digestive Diseases and Sciences, Vol. 52, No. 11, 11.2007, p. 3145-3148.

Research output: Contribution to journalArticle

Akatsu, Tomotaka ; Aiura, Koichi ; Ito, Yasuhiro ; Ueda, Masakazu ; Kameyama, Kaori ; Kitajima, Masaki. / A Novel Von Hippel-Lindau case with germline mutation at codon 167 (CGG to TGG) having endocrine microadenomatosis of the pancreas. In: Digestive Diseases and Sciences. 2007 ; Vol. 52, No. 11. pp. 3145-3148.
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