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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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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Schneider, P M, Carroll, M C, Alper, C A, Rittner, C, Whitehead, A S, Yunis, E J, Colten, H R
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1986
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC423642/
https://ncbi.nlm.nih.gov/pubmed/3018042
Etiketler: Etiketle
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