Brain Transcriptome Database (BrainTx)http://rdf.ncbi.nlm.nih.gov/pubmed/

Angela. Goytain, et.al., NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter., The Journal of biological chemistry, 2007, 282
http://rdf.ncbi.nlm.nih.gov/pubmed/17166836

Angela. Goytain, et.al., NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter., The Journal of biological chemistry, 2007, 282

http://rdf.ncbi.nlm.nih.gov/pubmed/

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