Clinical, Genetic and Functional Characteristics of Three NovelCYP17A1Mutations Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency

Published 2010 View Full Article

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Title
Clinical, Genetic and Functional Characteristics of Three NovelCYP17A1Mutations Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency
Authors
Keywords
-
Journal
Hormone Research in Paediatrics
Volume 73, Issue 3, Pages 198-204
Publisher
S. Karger AG
Online
2010-03-03
DOI
10.1159/000284362

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