Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption

Antzeko izenburuak

• Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption
  nork: Shin, Daniel Sanghoon, et al.
  Argitaratua: (2010)
• Role of the tryptophan residues in proton-coupled folate transporter (PCFT-SLC46A1) function
  nork: Najmi, Mitra, et al.
  Argitaratua: (2016)
• Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption
  nork: Shin, Daniel Sanghoon, et al.
  Argitaratua: (2011)
• The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption
  nork: Zhao, Rongbao, et al.
  Argitaratua: (2016)
• Identification of a functionally critical GXXG motif and its relationship to the folate binding site of the proton-coupled folate transporter (PCFT-SLC46A1)
  nork: Zhao, Rongbao, et al.
  Argitaratua: (2012)