Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

Cell

Volumn 73, Issue 4, 1993, Pages 703-711

  Takeda, Junji ^a   Miyata, Toshio ^a   Kawagoe, Kazuyoshi ^a   Iida, Yoshiyasu ^a,b   Endo, Yuichi ^c   Fujita, Teizo ^c   Takahashi, Minoru ^a   Kitani, Teruo ^a   Kinoshita, Taroh ^a  

^a OSAKA UNIVERSITY   (Japan)

^b NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c FUKUSHIMA MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE PROTEIN; COMPLEMENTARY DNA; GLYCOSYLPHOSPHATIDYLINOSITOL;

ARTICLE; B LYMPHOCYTE; CASE REPORT; GRANULOCYTE; HUMAN; HUMAN CELL; NORTHERN BLOTTING; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PRIORITY JOURNAL; SOMATIC MUTATION;

B-LYMPHOCYTES; BASE SEQUENCE; CELL LINE; EXONS; GLYCOSYLPHOSPHATIDYLINOSITOLS; HEMATOPOIETIC STEM CELLS; HEMOGLOBINURIA, PAROXYSMAL; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; RNA SPLICING; RNA, MESSENGER; SEQUENCE DELETION; SUPPORT, NON-U.S. GOV'T; TRANSFECTION; X CHROMOSOME;

EID: 0027310539     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(93)90250-T     Document Type: Article

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