Art

J-GLOBAL ID：200902168013791228   Reference number：96A0564648

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.

Ankyrin-1の突然変異は優性及び劣性の遺伝性球状赤血球症の主な原因となる

Author (9)： EBER S W (Harvard Medical School, Massachusetts, USA) ,  GONZALEZ J M (Harvard Medical School, Massachusetts, USA) ,  LUX M L (Harvard Medical School, Massachusetts, USA) ,  SCARPA A L (Yale Univ. School of Medicine, Connecticut, USA) ,  TSE W T (Yale Univ. School of Medicine, Connecticut, USA) ,  DORNWELL M (Univ. Kinderklinik, Goettingen) ,  GALLAGHER P G (Yale Univ. School of Medicine, Connecticut, USA) ,  FORGET B G (Yale Univ. School of Medicine, Connecticut, USA) ,  LUX S E (Harvard Medical School, Massachusetts, USA)
Material： Nature Genetics  (Nat Genet)
Volume： 13  Issue： 2  Page： 214-218  Publication year： Jun. 1996 
JST Material Number： W0430A  ISSN： 1061-4036  Document type： Article
Article type： 短報  Country of issue： United States (USA)  Language： ENGLISH (EN)

Thesaurus term： hemolytic anemia ,...
Semi thesaurus term： hereditary spherocytosis ,...

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JST classification (2)： Basic hematology  (GK01020N) ,  Molecular genetics in general  (EC02010J)

Terms in the title (4)： 突然変異 ,  劣性 ,  遺伝性球状赤血球症 ,  原因