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Summary Expression Phenotypes Gene Literature (34) GO Terms (6) Nucleotides (141) Proteins (58) Interactants (206) Wiki
XB--6462483

Papers associated with mag (and Disease Ontology)



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NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter., Goytain A, Hines RM, El-Husseini A, Quamme GA., J Biol Chem. March 16, 2007; 282 (11): 8060-8.          

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