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Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.

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Title: Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.
Authors: Akcan, Neşe1 nese.akcan@med.neu.edu.tr, Uyguner, Oya2, Baş, Firdevs3, Altunoğlu, Umut2,4, Toksoy, Güven2, Karaman, Birsen2, Avcı, Şahin2,4, Abalı, Zehra Yavaş3, Poyrazoğlu, Şükran3, Aghayev, Agharza2, Karaman, Volkan2, Bundak, Rüveyde5, Başaran, Seher2, Darendeliler, Feyza3
Source: Journal of Clinical Research in Pediatric Endocrinology. Jun2022, Vol. 14 Issue 2, p153-171. 19p.
Database: Academic Search Ultimate
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  Data: Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Clinical+Research+in+Pediatric+Endocrinology%22">Journal of Clinical Research in Pediatric Endocrinology</searchLink>. Jun2022, Vol. 14 Issue 2, p153-171. 19p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=157332833
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      – Type: doi
        Value: 10.4274/jcrpe.galenos.2022.2021-9-19
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      – Code: eng
        Text: English
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        PageCount: 19
        StartPage: 153
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      – TitleFull: Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.
        Type: main
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            – D: 01
              M: 06
              Text: Jun2022
              Type: published
              Y: 2022
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            – TitleFull: Journal of Clinical Research in Pediatric Endocrinology
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