Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras

Detalles Bibliográficos
Autores principales: Lao, Qizong, Merke, Deborah P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298381/
https://www.ncbi.nlm.nih.gov/pubmed/33824469
http://dx.doi.org/10.1038/s41431-021-00870-5
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author Lao, Qizong
Merke, Deborah P.
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Merke, Deborah P.
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spelling pubmed-82983812021-08-05 Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras Lao, Qizong Merke, Deborah P. Eur J Hum Genet Correspondence Springer International Publishing 2021-04-07 2021-07 /pmc/articles/PMC8298381/ /pubmed/33824469 http://dx.doi.org/10.1038/s41431-021-00870-5 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Correspondence
Lao, Qizong
Merke, Deborah P.
Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
title Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
title_full Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
title_fullStr Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
title_full_unstemmed Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
title_short Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
title_sort molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include cah-x chimeras
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298381/
https://www.ncbi.nlm.nih.gov/pubmed/33824469
http://dx.doi.org/10.1038/s41431-021-00870-5
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