Chimeric Genes Causing 11β-Hydroxylase Deficiency: Implications in Clinical and Molecular Diagnosis
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40291-024-00697-y.pdf
Reference33 articles.
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2. Falhammar H, Thoren M. Clinical outcomes in the management of congenital adrenal hyperplasia. Endocrine. 2012;41:355–73. https://doi.org/10.1007/s12020-011-9591-x.
3. Bulsari K, Falhammar H. Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Endocrine. 2017;55:19–36. https://doi.org/10.1007/s12020-016-1189-x.
4. White PC, Speiser PW. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev. 2000;21:245–91. https://doi.org/10.1210/edrv.21.3.0398.
5. Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet. 2005;365:2125–36. https://doi.org/10.1016/S0140-6736(05)66736-0.
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