Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.

DNA was analysed from 20 patients with congenital adrenal hyperplasia due to cytochrome P-450 steroid 21-hydroxylase deficiency. Using probes recognising sequences in both the 21-hydroxylase gene and the adjacent fourth component of complement (C4), one patient was found to have a homozygous deletio...

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Autores principales: Rumsby, G, Carroll, M C, Porter, R R, Grant, D B, Hjelm, M
Formato: Artigo
Lenguaje:Inglês
Publicado: 1986
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Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049628/
https://ncbi.nlm.nih.gov/pubmed/3487654
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