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Results 1 - 4 of 4 for arabian
  1. HMGCL gene 
    ... example, the most common mutation in the Saudi Arabian population replaces the amino acid arginine with the ...
    https://medlineplus.gov/genetics/gene/hmgcl - Genetics
  2. SLC5A1 gene 
    ... Ramzan K, Imtiaz F. SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption. J Pediatr ...
    https://medlineplus.gov/genetics/gene/slc5a1 - Genetics
  3. HPSE2 gene 
    ... identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome. J Pediatr Urol. ...
    https://medlineplus.gov/genetics/gene/hpse2 - Genetics
  4. CYP2R1 gene 
    ... CYP2R1 vitamin D 25-hydroxylase in a Saudi Arabian family with severe vitamin D deficiency. J Clin ...
    https://medlineplus.gov/genetics/gene/cyp2r1 - Genetics