Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module): A mechanism for gene deletions and disease associations

Journal of Biological Chemistry

Volumn 274, Issue 17, 1999, Pages 12147-12156

  Yang, Zhenyu ^a,b   Mendoza, Anna R ^a   Welch, Thomas R ^c   Zipf, William B ^a,b   Yung Yu, C ^a,b  

^a NATIONWIDE CHILDREN S HOSPITAL   (United States)

^b OHIO STATE UNIVERSITY   (United States)

^c UNIVERSITY OF CINCINNATI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C4; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 3; PROTEIN SERINE THREONINE KINASE; STEROID 21 MONOOXYGENASE; TENASCIN;

ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; DNA CLEAVAGE; DNA SEQUENCE; GENE DELETION; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; PSEUDOGENE;

ADRENAL HYPERPLASIA, CONGENITAL; ARTHRITIS, JUVENILE RHEUMATOID; BASE SEQUENCE; COMPLEMENT C4; DNA; GENE DELETION; GENE DUPLICATION; HUMANS; MAJOR HISTOCOMPATIBILITY COMPLEX; MOLECULAR SEQUENCE DATA; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE HOMOLOGY, NUCLEIC ACID; STEROID 21-HYDROXYLASE; TENASCIN; TUMOR CELLS, CULTURED;

EID: 0033597231     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.274.17.12147     Document Type: Article

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