Art

J-GLOBAL ID：200902052188924095   Reference number：90A0686473

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.

第8染色体上のヒト赤血球アンキリン遺伝子欠失を伴なう遺伝性球状赤血球症

Author (9)： LUX S E (Harvard Medical School, Massachusetts, USA) ,  TSE W T (Yale Univ. School of Medicine, Connecticut, USA) ,  MENNINGER J C (Yale Univ. School of Medicine, Connecticut, USA) ,  JOHN K M (Harvard Medical School, Massachusetts, USA) ,  HARRIS P (Harvard Medical School, Massachusetts, USA) ,  SHALEV O (Harvard Medical School, Massachusetts, USA) ,  CHILCOTE R R (Univ. California at Irvine School of Medicine, California, USA) ,  MARCHESI S L (Yale Univ. School of Medicine, Connecticut, USA) ,  FORGET B G
Material： Nature (London)  (Nature (Lond))
Volume： 345  Issue： 6277  Page： 736-739  Publication year： Jun. 21, 1990 
JST Material Number： D0193B  ISSN： 0028-0836  Document type： Article
Article type： 短報  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： human ,...
Semi thesaurus term： spherocytosis

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JST classification (2)： Structure and chemistry of genes  (EC02020U) ,  Hematologic diseases  (GK03000F)

Terms in the title (6)： 第8染色体 ,  ヒト ,  赤血球 ,  アンキリン ,  遺伝子欠失 ,  遺伝性球状赤血球症