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Volumn 268, Issue 5215, 1995, Pages 1347-1349
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Mutations in fas associated with human lymphoproliferative syndrome and autoimmunity
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Author keywords
[No Author keywords available]
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Indexed keywords
CELL SURFACE RECEPTOR;
APOPTOSIS;
ARTICLE;
AUTOIMMUNITY;
CASE REPORT;
CONTROLLED STUDY;
ETIOLOGY;
FEMALE;
GENE DELETION;
HUMAN;
HUMAN CELL;
LYMPHOPROLIFERATIVE DISEASE;
MALE;
PRIORITY JOURNAL;
AMINO ACID SEQUENCE;
ANTIGENS, CD95;
ANTIGENS, SURFACE;
APOPTOSIS;
AUTOIMMUNE DISEASES;
BASE SEQUENCE;
CHILD;
FEMALE;
FRAMESHIFT MUTATION;
HUMAN;
INFANT;
LYMPHOPROLIFERATIVE DISORDERS;
MALE;
MOLECULAR SEQUENCE DATA;
SEQUENCE DELETION;
SUPPORT, NON-U.S. GOV'T;
SYNDROME;
THROMBOCYTOPENIA;
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EID: 0029006893
PISSN: 00368075
EISSN: None
Source Type: Journal
DOI: 10.1126/science.7539157 Document Type: Article |
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Times cited : (1194)
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References (17)
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