Data on the functional consequences of the mutations identified in 21-Hydroxylase deficient CAH patients

This article presents the data set regarding the functional characterization of mutations in CYP21A2 gene in CAH patients as described in “Functional characterization and molecular modeling of the mutations in CYP21A2 gene from patients with Congenital Adrenal Hyperplasia (Khajuria et al., 2018) [1]...

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Detalles Bibliográficos
Autores principales: Khajuria, Ragini, Walia, Rama, Bhansali, Anil, Prasad, Rajendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Proteomics and Biochemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993105/
https://www.ncbi.nlm.nih.gov/pubmed/29892641
http://dx.doi.org/10.1016/j.dib.2018.05.043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993105/
https://www.ncbi.nlm.nih.gov/pubmed/29892641
http://dx.doi.org/10.1016/j.dib.2018.05.043

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