Mutational Analysis of 12 Patients with the Phenotype of Ehlers-Danlos Syndrome Type VIB Shows no Linkage to the Zinc Transporter Gene SLC39A13

مواد مشابهة

• Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13
  بواسطة: Giunta, Cecilia, وآخرون
  منشور في: (2008)
• Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) and the mutant zinc transporter ZIP13
  بواسطة: Bin, Bum-Ho, وآخرون
  منشور في: (2014)
• Promotion of vesicular zinc efflux by ZIP13 and its implications for spondylocheiro dysplastic Ehlers–Danlos syndrome
  بواسطة: Jeong, Jeeyon, وآخرون
  منشور في: (2012)
• The SLC39 family of zinc transporters
  بواسطة: Jeong, Jeeyon, وآخرون
  منشور في: (2013)
• The Connective Tissue Disorder Associated with Recessive Variants in the SLC39A13 Zinc Transporter Gene (Spondylo-Dysplastic Ehlers–Danlos Syndrome Type 3): Insights from Four Novel Patients and Follow-Up on Two Original Cases
  بواسطة: Kumps, Camille, وآخرون
  منشور في: (2020)