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Volumn 113, Issue 4, 1997, Pages 1384-1389
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Pas/APO1 mutations and autoimmune lymphoproliferative syndrome in a patient with type 2 autoimmune hepatitis
a a a a a a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
CD3 ANTIGEN;
CD4 ANTIGEN;
CD8 ANTIGEN;
FAS ANTIGEN;
AUTOANTIBODY;
IMMUNOGLOBULIN A;
IMMUNOGLOBULIN G;
IMMUNOGLOBULIN M;
ARTICLE;
AUTOIMMUNE HEPATITIS;
CASE REPORT;
CHILD;
CHILDHOOD DISEASE;
FEMALE;
GENE MUTATION;
HEPATOSPLENOMEGALY;
HUMAN;
LIVER DISEASE;
LYMPHOPROLIFERATIVE DISEASE;
PRIORITY JOURNAL;
SYNDROME DELINEATION;
ALLELE;
APOPTOSIS;
AUTOIMMUNE DISEASE;
BLOOD;
COMPARATIVE STUDY;
GENETICS;
HEPATITIS;
HEPATOMEGALY;
IMMUNOLOGY;
LIVER FUNCTION TEST;
MALE;
PATHOLOGY;
PEDIGREE;
POINT MUTATION;
PRESCHOOL CHILD;
SPLENOMEGALY;
SYNDROME;
T LYMPHOCYTE SUBPOPULATION;
ALLELES;
ANTIGENS, CD95;
APOPTOSIS;
AUTOANTIBODIES;
AUTOIMMUNE DISEASES;
CHILD, PRESCHOOL;
FEMALE;
HEPATITIS;
HEPATOMEGALY;
HUMANS;
IMMUNOGLOBULIN A;
IMMUNOGLOBULIN G;
IMMUNOGLOBULIN M;
LIVER FUNCTION TESTS;
LYMPHOPROLIFERATIVE DISORDERS;
MALE;
PEDIGREE;
POINT MUTATION;
SPLENOMEGALY;
SYNDROME;
T-LYMPHOCYTE SUBSETS;
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EID: 0030610755
PISSN: 00165085
EISSN: None
Source Type: Journal
DOI: 10.1053/gast.1997.v113.pm9322534 Document Type: Article |
Times cited : (57)
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References (20)
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