Growth Hormon Deficiency in Identical Twins with Gitelman Syndrome Due to Compound Heterozygous Mutation (p.R80fs*35/p.K957X) of the SLC12A3 Gene and the Evaluation of the Response to Growth Hormone Replacement Therapy
HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.461-462, 2018 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Özet
- Cilt numarası: 90
- Basım Tarihi: 2018
- Dergi Adı: HORMONE RESEARCH IN PAEDIATRICS
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.461-462
- Hacettepe Üniversitesi Adresli: Evet