Comparing the Southern blot method and polymerase chain reaction product analysis for chimeric RCCX detection in CYP21A2 deficiency-Reference-Cited by-同舟云学术

Comparing the Southern blot method and polymerase chain reaction product analysis for chimeric RCCX detection in CYP21A2 deficiency

Published:2010-04 Issue:2 Volume:399 Page:293-298
ISSN:0003-2697
Container-title:Analytical Biochemistry
language:en
Short-container-title:Analytical Biochemistry

Author:

Lee Hsien-Hsiung,Lee Yann-Jinn,Chao Mei-Chyn

Funder

Mackay Memorial Hospital of Taiwan

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference34 articles.

1. Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene duplication.

2. Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus;Gitelman;Mol. Cell Biol.,1992

3. Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B;Bristow;J. Cell Biol.,1993

4. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in Caucasians: the load of RCCX genetic diversity on major histocompatibility complex-associated disease;Blanchong;J. Exp. Med.,2000

5. The complete exon–intron structure of a human complement component C4A gene: DNA sequences, polymorphism, and linkage to the 21-hydroxylase genes;Yu;J. Immunol.,1991

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