Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
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Özgün Araştırma
CİLT: 8 SAYI: 2
P: 218 - 223
Haziran 2016

Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency

J Clin Res Pediatr Endocrinol 2016;8(2):218-223
1. Harran University Faculty Of Medicine, Department Of Pediatric Endocrinology, Şanlıurfa, Turkey
2. Sıtkı Koçman University Faculty Of Health Sciences, Department Of Medical Biology, Muğla, Turkey
3. Uludağ University Faculty Of Medicine, Department Of Pediatrics, Bursa, Turkey
4. Bülent Ecevit University Faculty Of Medicine, Department Of Medical Genetics, Zonguldak, Turkey
Bilgi mevcut değil.
Bilgi mevcut değil
Alındığı Tarih: 14.10.2015
Kabul Tarihi: 12.01.2016
Yayın Tarihi: 06.06.2016
E-Pub Tarihi: 12.01.2016
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