14

عناصر مشابهة

• Assay Development for the Detection of FGF23 Mutations That Cause Familial Tumoral Calcinosis by Amplification Refractory Mutation System (ARMS)
  بواسطة: Al Ghamdi, Manal Abd Allah S. منشور: (2011)
• FGF23 Loss of Function Mutations Cause a Structural Alteration and Misfolding in the Secreted Hormone
  بواسطة: العفاسي، سارة عبدالله حمود منشور: (2017)
• Identification and Characterization of Mutations in Genes Implicated in Familial Hyperchlosterolaemia in Omani Families
  بواسطة: Al-Zidi, Ward Al-Muna Ali Rashid منشور: (2013)
• Mutation Analysis of the Low Density Lipoprotein Receptor Gene in Clinically Diagnosed Arab Family with Familial Hypercholesterolemia
  بواسطة: القلاف، هالة ماجد سلطان منشور: (2011)
• Identification of Novel Disease-Causing Gene Mutations Detected by Whole-Exome Sequencing and Whole - Genome Sequencing in Palestinian Families with Rare Diseases
  بواسطة: Alshaer, Shurouq Abdullah Yaghnam منشور: (2022)