Kheirollahi, Majid

• Vol 21: April 2016 - Original Article
  Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot
  Abstract  PDF
• Vol 22: March 2017 - Short Communication
  Report of SLC3A1/rBAT gene mutations in Iranian cystinuria patients: A direct sequencing study
  Abstract  PDF
• Vol 24: APRIL (2019) - Original Article
  The MTHFR C677T polymorphism influences the efficacy of folic acid supplementation on the nerve conduction studies in patients with diabetic polyneuropathy; A randomized, double blind, placebo-controlled study
  Abstract  PDF