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
  • Product Usage:
  • ID: PN59419
Catalog #s
A11001
A11004
A11008
A11029
A11031
A11034
A11045
A12380
A21049
A22281
M1290
c213877427b46fa96cff6c39e837ccee_Citations