Author:
Manfras Burkhard J.,Swinyard Michael,Rudert William A.,Ball Edward J.,Lee Peter A.,K�hnl Peter,Trucco Massimo,B�hm Bernhard O.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference21 articles.
1. Amor M, Parker KL, Globermann H (1988) Mutation in the CYP21B gene (Ile-172-Asp). Proc Natl Acad Sci USA 85:1600?1604
2. Boehm BO, Rosak C, Boehm TLJ, et al (1986) Classical and lateonset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21 -OH gene region. Mol Biol Med 3:437?448
3. Bouchard P, Kuttenn F, Mowszowicz I, Schaison G, Raux-Eurin MC, Mauvais-Jarvis P (1981) Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. Acta Endocrinol (Copenh) 96:107?110
4. Carroll MC, Pasldottir A, Belt KT, Porter RR (1985) Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region. EMBO J 4:2547?2552
5. Donohoue PA, Dop CV, McLean RH, et al (1986) Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein. J Clin Endocrinol Metab 62:995?1002
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献