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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...

詳細記述

保存先:
書誌詳細
主要な著者: Schneider, P M, Carroll, M C, Alper, C A, Rittner, C, Whitehead, A S, Yunis, E J, Colten, H R
フォーマット: Artigo
言語:Inglês
出版事項: 1986
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC423642/
https://ncbi.nlm.nih.gov/pubmed/3018042
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