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Literature for DOID 607: paraplegia
Xenbase Articles

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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):1083-351X.
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