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

  • Authors: Goytain A, Hines RM, El-Husseini A, Quamme GA
  • Journal: J Biol Chem (2007) 282:8060-8068
  • PubMed ID: 17166836