A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report

相似書籍

• Creatine transporter deficiency, an underdiagnosed cause of male intellectual disability
  由: Jangid, Neha, et al.
  出版: (2020)
• A novel SLC6A8 mutation associated with motor dysfunction in a child exhibiting creatine transporter deficiency
  由: Cervera-Acedo, Cristina, et al.
  出版: (2015)
• X-Linked Creatine-Transporter Gene (SLC6A8) Defect: A New Creatine-Deficiency Syndrome
  由: Salomons, Gajja S., et al.
  出版: (2001)
• Treatment efficacy of high‐dose creatine supplementation in a child with creatine transporter (SLC6A8) deficiency
  由: Shi, Kaili, et al.
  出版: (2021)
• Upregulation of the Creatine Transporter Slc6A8 by Klotho
  由: Ahmad Almilaji, et al.
  出版: (2014-11-01)