Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.

Several autoimmune disorders as well as congenital adrenal hyperplasia (CAH) are either associated or closely linked with genetic variants of the fourth component of complement (C4A and C4B) and the enzyme steroid 21-hydroxylase (21-OH). These proteins are encoded by genes that are located downstrea...

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Detalles Bibliográficos
Publicado en:J Clin Invest
Autores principales: Schneider, P M, Carroll, M C, Alper, C A, Rittner, C, Whitehead, A S, Yunis, E J, Colten, H R
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Clinical Investigation 1986
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423642/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3018042/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112623
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