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. |
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| 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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