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

Internet

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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