SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6

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Summary

Literature (1)

Literature for OMIM 600363: SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6

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.

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.