X chromosome inactivation and female predisposition to autoimmunity

Clinical Reviews in Allergy and Immunology

Volumn 34, Issue 3, 2008, Pages 348-351

  Ozcelik, Tayfun ^a  

^a BILKENT UNIVERSITY   (Turkey)

Author keywords

Autoimmune diseases; Female predisposition; Mosaicism; X chromosome inactivation

Indexed keywords

ANDROGEN RECEPTOR; MELANOMA ANTIGEN;

AUTOIMMUNE DISEASE; AUTOIMMUNITY; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE PREDISPOSITION; DUCHENNE MUSCULAR DYSTROPHY; FRAGILE X SYNDROME; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENETIC TRAIT; GENETIC VARIABILITY; HEMATOPOIETIC STEM CELL; HETEROZYGOSITY; HUMAN; IMMUNOLOGICAL TOLERANCE; REVIEW; SCLERODERMA; WISKOTT ALDRICH SYNDROME; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKED DISORDER; X LINKED AGAMMAGLOBULINEMIA; X LINKED MENTAL RETARDATION;

AUTOIMMUNE DISEASES; AUTOIMMUNITY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MUTATION; SCLERODERMA, SYSTEMIC; SEX CHARACTERISTICS; X CHROMOSOME INACTIVATION;

EID: 49349084347     PISSN: 10800549     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12016-007-8051-0     Document Type: Review

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