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Harada, F., Kimura, A., Iwanaga, T., Shimozawa, K., Yata, J., Sasazuki, T. (1987) Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Proceedings of the National Academy of Sciences, 84 (22) 8091-8094 doi:10.1073/pnas.84.22.8091

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Reference TypeJournal (article/letter/editorial)
TitleGene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
JournalProceedings of the National Academy of Sciences
AuthorsHarada, F.Author
Kimura, A.Author
Iwanaga, T.Author
Shimozawa, K.Author
Yata, J.Author
Sasazuki, T.Author
Year1987 (November 1)Volume84
Issue22
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.84.22.8091Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1462059Long-form Identifiermindat:1:5:1462059:5
GUID0
Full ReferenceHarada, F., Kimura, A., Iwanaga, T., Shimozawa, K., Yata, J., Sasazuki, T. (1987) Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Proceedings of the National Academy of Sciences, 84 (22) 8091-8094 doi:10.1073/pnas.84.22.8091
Plain TextHarada, F., Kimura, A., Iwanaga, T., Shimozawa, K., Yata, J., Sasazuki, T. (1987) Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Proceedings of the National Academy of Sciences, 84 (22) 8091-8094 doi:10.1073/pnas.84.22.8091
In(1987, November) Proceedings of the National Academy of Sciences Vol. 84 (22) Proceedings of the National Academy of Sciences

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(1987) Correction: P450XXI (steroid 21-hydroxylase) Gene Deletions are not Found in Family Studies of Congenital Adrenal Hyperplasia. Proceedings of the National Academy of Sciences, 84 (22) 8054 doi:10.1073/pnas.84.22.8054
Matteson, K. J., Phillips, J. A., Miller, W. L., Chung, B. C., Orlando, P. J., Frisch, H., Ferrandez, A., Burr, I. M. (1987) P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia. Proceedings of the National Academy of Sciences, 84 (16) 5858-5862 doi:10.1073/pnas.84.16.5858
Higashi, Y., Tanae, A., Inoue, H., Hiromasa, T., Fujii-Kuriyama, Y. (1988) Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products. Proceedings of the National Academy of Sciences, 85 (20) 7486-7490 doi:10.1073/pnas.85.20.7486
New, M. I., Wilson, R. C. (1999) Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess. Proceedings of the National Academy of Sciences, 96 (22) 12790-12797 doi:10.1073/pnas.96.22.12790
Haglund-Stengler, B., Martin Ritzen, E., Gustafsson, J., Luthman, H. (1991) Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency. Proceedings of the National Academy of Sciences, 88 (19) 8352-8356 doi:10.1073/pnas.88.19.8352
New, M. I., Abraham, M., Gonzalez, B., Dumic, M., Razzaghy-Azar, M., Chitayat, D., Sun, L., Zaidi, M., Wilson, R. C., Yuen, T. (2013) Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Proceedings of the National Academy of Sciences, 110 (7) 2611-2616 doi:10.1073/pnas.1300057110
White, P. C., New, M. I., Dupont, B. (1984) HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. Proceedings of the National Academy of Sciences, 81 (23) 7505-7509 doi:10.1073/pnas.81.23.7505
Nimkarn, Saroj, New, Maria I. (2010) Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Annals of the New York Academy of Sciences, 1192 (1) 5-11 doi:10.1111/j.1749-6632.2009.05225.x
Hornsby, P. J., Hancock, J. P., Vo, T. P., Nason, L. M., Ryan, R. F., McAllister, J. M. (1987) Loss of expression of a differentiated function gene, steroid 17 alpha-hydroxylase, as adrenocortical cells senescence in culture. Proceedings of the National Academy of Sciences, 84 (6) 1580-1584 doi:10.1073/pnas.84.6.1580
Shiroishi, T., Sagai, T., Natsuume-Sakai, S., Moriwaki, K. (1987) Lethal deletion of the complement component C4 and steroid 21-hydroxylase genes in the mouse H-2 class III region, caused by meiotic recombination. Proceedings of the National Academy of Sciences, 84 (9) 2819-2823 doi:10.1073/pnas.84.9.2819
Amor, M., Parker, K. L., Globerman, H., New, M. I., White, P. C. (1988) Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency. Proceedings of the National Academy of Sciences, 85 (5) 1600-1604 doi:10.1073/pnas.85.5.1600
 
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