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

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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Bibliographic Details
Main Authors: Ragini Khajuria, Rama Walia, Anil Bhansali, Rajendra Prasad
Format: Article
Language:English
Published: Elsevier 2017-02-01
Series:Data in Brief
Subjects:
CYP21A2 gene
Salt wasting
Simple virilizing
Non classical
Known mutations
Novel mutations
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340916307740

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http://www.sciencedirect.com/science/article/pii/S2352340916307740

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