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Three human aminoacyl-tRNA synthetases have distinct sub-mitochondrial localizations that are unaffected by disease-associated mutations

The Journal of biological chemistry, 31 August 2018, Vol.293(35), pp.13604-13615 [Peer Reviewed Journal]

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Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency

BBA - Molecular Basis of Disease, August 2013, Vol.1832(8), pp.1304-1312 [Peer Reviewed Journal]

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TMEM126A is a mitochondrial located mRNA (MLR) protein of the mitochondrial inner membrane

BBA - General Subjects, June 2013, Vol.1830(6), pp.3719-3733 [Peer Reviewed Journal]

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Redistribution of accumulated cell iron: a modality of chelation with therapeutic implications.

Blood, February 1, 2008, Vol.111(3), pp.1690-1699 [Peer Reviewed Journal]

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Spinal muscular atrophy diagnostic methods

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SPINAL MUSCULAR ATROPHY DIAGNOSTIC METHODS

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Survival motor Neurons (SMN) gene: a gene for spinal muscular atrophy

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Survival motor neurons (SMN) gene: a gene for spinal muscular atrophy

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Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts

BBA - Molecular Basis of Disease, December 2013, Vol.1832(12), pp.2103-2114 [Peer Reviewed Journal]

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