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Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

The HLA-linked human steroid 21-hydroxylase gene CYP21B and its closely homologous pseudogene CYP21A are each normally located centromeric to a fourth component of complement (C4) gene, C4B and C4A, respectively, in an organization suggesting tandem duplication of a ca. 30-kilobase DNA unit containi...

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Sparad:
I publikationen:Proc Natl Acad Sci U S A
Huvudupphov: Sinnott, P, Collier, S, Costigan, C, Dyer, P A, Harris, R, Strachan, T
Materialtyp: Artigo
Språk:Inglês
Utgiven: National Academy of Sciences 1990
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC53635/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2315306/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.6.2107
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