Special stain and X-ray probe microanalysis of livers with Wilson disease

HAYASHI Hisao; FUJITA Yoshikazu; TATSUMI Yasuaki; HATTORI Ai; HAYASHI Kazuhiko; KATANO Yoshiaki; WAKUSAWA Shinya; YANO Motoyoshi; ITOH Masafumi; MIZUTANI Naoki; GOTO Hidemi

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J-GLOBAL ID：200902284434463785 Reference number：09A0746284

Special stain and X-ray probe microanalysis of livers with Wilson disease

Wilson病における肝臓の特殊染色及びX線プローブ微小分析

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Material：
Volume： 39 Issue： 6 Page： 563-568 Publication year： Jun. 2009
JST Material Number： W1284A ISSN： 1386-6346 Document type： Article
Article type：原著論文 Country of issue： Australia (AUS) Language： ENGLISH (EN)

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Digestive system diseases , Congenital diseases,deformities in general.

Reference (18)：

TANZI, RE. The Wilson disease gene is a copper transporting atpase with homology to the Menkes disease gene. Nat Genet. 1993, 5, 344-350
BULL, PC. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat Genet. 1993, 5, 327-337
YAMAGUCHI, Y. Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease. Biochem Biophys Res Commun. 1993, 197, 271-277
FERENCI, P. Diagnosis and phenotypic classification of Wilson disease. Liver Int. 2003, 23, 139-142
GITLIN, JD. Wilson disease. Gastroenterology. 2003, 125, 1868-1877

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