Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

Схожие документы

• Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption
  по: Shin, Daniel Sanghoon, et al.
  Опубликовано: (2012)
• Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1
  по: Aluri, Srinivas, et al.
  Опубликовано: (2018)
• Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption
  по: Shin, Daniel Sanghoon, et al.
  Опубликовано: (2011)
• The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption
  по: Zhao, Rongbao, et al.
  Опубликовано: (2016)
• Role of the tryptophan residues in proton-coupled folate transporter (PCFT-SLC46A1) function
  по: Najmi, Mitra, et al.
  Опубликовано: (2016)