NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter.

Citations & References

  • Authors: Goytain A, Hines RM, El-Husseini A, Quamme GA
  • Journal: J Biol Chem (2007) 282:8060-8068
  • ID: PN59419
c213877427b46fa96cff6c39e837ccee_Citations