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Results 1 - 10 of 18 for arabian
  1. Propionic acidemia 
    ... population of Greenland, some Amish communities, and Saudi Arabians. Mutations in the PCCA and PCCB genes cause ...
    https://medlineplus.gov/genetics/condition/propionic-acidemia - Genetics
  2. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 
    ... codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. Am J Hum Genet. 1998 Feb; ...
    https://medlineplus.gov/...oxy-3-methylglutaryl-coa-lyase-deficiency - Genetics
  3. Glucose-galactose malabsorption 
    ... Ramzan K, Imtiaz F. SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption. J Pediatr ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  4. Congenital fibrosis of the extraocular muscles 
    ... in only a few families of Turkish, Saudi Arabian, and Iranian descent. Tukel syndrome appears to be ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  5. Sickle cell disease 
    ... countries such as Greece, Turkey, and Italy; the Arabian Peninsula; India; and Spanish-speaking regions in South ...
    https://medlineplus.gov/genetics/condition/sickle-cell-disease - Genetics
  6. Ochoa syndrome 
    ... identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome. J Pediatr Urol. ...
    https://medlineplus.gov/genetics/condition/ochoa-syndrome - Genetics
  7. 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
  8. 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
  9. 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
  10. 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
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