(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

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Reference Type	Journal (article/letter/editorial)
Title	Correction: P450XXI (steroid 21-hydroxylase) Gene Deletions are not Found in Family Studies of Congenital Adrenal Hyperplasia
Journal	Proceedings of the National Academy of Sciences
Year	1987 (November 15)	Volume	84
Issue	22
Publisher	Proceedings of the National Academy of Sciences
DOI	doi:10.1073/pnas.84.22.8054Search in ResearchGate
	Generate Citation Formats
Mindat Ref. ID	1462021	Long-form Identifier	mindat:1:5:1462021:2
GUID	0
Full Reference	(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
Plain Text	(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
In	(1987, November) Proceedings of the National Academy of Sciences Vol. 84 (22) Proceedings of the National Academy of Sciences

	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
	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
	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
	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
	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
	White, P. C., Vitek, A., Dupont, B., New, M. I. (1988) Characterization of frequent deletions causing steroid 21-hydroxylase deficiency. Proceedings of the National Academy of Sciences, 85 (12) 4436-4440 doi:10.1073/pnas.85.12.4436
	*(1987) Correction: Tyrosine Hydroxylase is Expressed by Neocortical Neurons after Transplantation. Proceedings of the National Academy of Sciences, 84 (8) 2507 doi:10.1073/pnas.84.8.2507-a*
	Chung, B. C., Matteson, K. J., Miller, W. L. (1986) Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family. Proceedings of the National Academy of Sciences, 83 (12) 4243-4247 doi:10.1073/pnas.83.12.4243
	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
	Chung, B. C., Picado-Leonard, J., Haniu, M., Bienkowski, M., Hall, P. F., Shively, J. E., Miller, W. L. (1987) Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues. Proceedings of the National Academy of Sciences, 84 (2) 407-411 doi:10.1073/pnas.84.2.407
	Jack, H. M., Wabl, M. (1987) High rates of deletions in the constant region segment of the immunoglobulin mu gene. Proceedings of the National Academy of Sciences, 84 (14) 4934-4938 doi:10.1073/pnas.84.14.4934

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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

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