The G395R Mutation of the Sodium/Iodide Symporter (NIS) Gene in Patients with Dyshormonogenetic Congenital Hypothyroidism

類似資料

• Analysis of the T354P mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis
  著者:: Miranzadeh-Mahabadi, Hajar, 等
  出版事項: (2016)
• Association Study Between Metabolic Syndrome and rs8066560 Polymorphism in the Promoter Region of Sterol Regulatory Element-binding Transcription Factor 1 Gene in Iranian Children and Adolescents
  著者:: Miranzadeh-Mahabadi, Hajar, 等
  出版事項: (2016)
• Genetic Basis of the Metabolic Syndrome
  著者:: Hajar Miranzadeh-Mahabadi, 等
  出版事項: (2015-05-01)
• Absence of Association between -1131T>C Polymorphism in the Apolipoprotein APOA5 Gene and Pediatric Metabolic Syndrome
  著者:: Fatemi, Sayedeh Ghazaleh, 等
  出版事項: (2014)
• The Sodium-Iodide Symporter NIS and Pendrin in Iodide Homeostasis of the Thyroid
  著者:: Bizhanova, Aigerim, 等
  出版事項: (2009)