An AAVrh10-CAG-CYP21-HA vector allows persistent correction of 21-hydroxylase deficiency in a Cyp21−/− mouse model
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
https://www.nature.com/articles/gt201710.pdf
Reference19 articles.
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2. Bruining H, Bootsma AH, Koper JW, Bonjer J, de Jong FH, Lamberts SWJ . Fertility and body composition after laparoscopic bilateral adrenalectomy in a 30-year-old female with congenital adrenal hyperplasia. J Clin Endocrinol Metab 2001; 86: 482–484.
3. Loechner KJ, McLaughlin JT, Calikoglu AS . Alternative strategies for the treatment of classical congenital adrenal hyperplasia: pitfalls and promises. Int J Pediatr Endocrinol 2010; 2010: 1–10.
4. Gastaud F, Bouvattier C, Duranteau L, Brauner R, Thibaud E, Kutten F et al. Impaired sexual and reproductive outcomes in women with classical forms of congenital adrenal hyperplasia. J Clin Endocrinol Metab 2007; 92: 1391–1396.
5. Riepe FG, Tatzel S, Sippell WG, Pleiss J, Krone N . Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice. Endocrinology 2005; 146: 2563–2574.
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