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XB-GENEPAGE-961418
Papers associated with nipa1
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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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