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Impaired axonal mitochondrial movement and positioning found in different models of cmt disease 20 49 55 56 may affect multiple mitochondrial functions gdap1 silencing in neuroblastoma cells or genetic disruption in mice caused a similar change in ca 2 homeostasis.
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High resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116 204 snps.
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A failure to activate the store operated calcium entry soce process 20.
Ca 2 deregulation in gdap1 related cmt disease.
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