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Summary Literature (1)
Literature for DOID 607: paraplegia

Xenbase Articles :
( Denotes literature images)
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.