Expression data from the spinal cord of dmy rat with Mrs2 mutation

The demyelination (dmy) rat is a unique spontaneous myelin mutation that exhibits severe myelin breakdown with a late onset of clinical signs. The causative autosomal recessive mutation has been identified at the MRS2 magnesium transporter (Mrs2) gene, which encodes an essential component of the major Mg2+ influx system in mitochondria.

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Shimotsuma Y, Tanaka M, Izawa T, Yamate J, Kuwamura M