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A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation

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Published in:Journal of clinical research in pediatric endocrinology 2017-06, Vol.9 (2), p.2
Main Authors: Abur, Ummet, Atmaca, Aysegul, Scott, Hamish, Gagliardi, Lucia, Altundag, Engin, Akar, Omer Salih, Bayrak, Ilkay Koray, Ogur, Gonul
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container_title Journal of clinical research in pediatric endocrinology
container_volume 9
creator Abur, Ummet
Atmaca, Aysegul
Scott, Hamish
Gagliardi, Lucia
Altundag, Engin
Akar, Omer Salih
Bayrak, Ilkay Koray
Ogur, Gonul
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ispartof Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.2
issn 1308-5727
language eng
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source Open Access: PubMed Central; Publicly Available Content Database (Proquest) (PQ_SDU_P3)
subjects Care and treatment
Cytochrome P-450
Deficiency diseases
Development and progression
Gene mutation
Genetic aspects
Health aspects
title A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation
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