Data on the 21-Hydroxylase deficient CAH patients and the identification of known/novel mutations in CYP21A2 gene

This article presents the dataset regarding spectrum of mutations in 21-Hydroxylase deficient CAH patients as described in “The spectrum of CYP21A2 mutations in Congenital Adrenal Hyperplasia in an Indian cohort” (R. Khajuria, R. Walia, A. Bhansali, R. Prasad, 2017) [1]. This dataset features about...

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Detalles Bibliográficos
Autores principales: Khajuria, Ragini, Walia, Rama, Bhansali, Anil, Prasad, Rajendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Data Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330408/
https://www.ncbi.nlm.nih.gov/pubmed/28275658
http://dx.doi.org/10.1016/j.dib.2016.12.013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330408/
https://www.ncbi.nlm.nih.gov/pubmed/28275658
http://dx.doi.org/10.1016/j.dib.2016.12.013

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