Matches in Nanopublications for { ?s ?p "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_assertion description "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666574.RAqfsZEMCFJzC_Cbw5Zi5Z3vpag4vmSmo74lfsBYv49Qs130_provenance.
- NP894861.RAfxD6Zm5irDTSIMy7vXJJIO8beGTjxhcKjQxHlMm2NyA130_assertion description "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894861.RAfxD6Zm5irDTSIMy7vXJJIO8beGTjxhcKjQxHlMm2NyA130_provenance.
- assertion description "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_assertion description "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866803.RAeyie1K6peiroY_dhgLfFAptAfWYYGVHVl3L5bkG7494130_provenance.
- NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_assertion description "[In addition, autosomal recessive mutations in the erythroid-specific mitochondrial transporter SLC25A38 and glutaredoxin 5 (GLRX5) have recently been identified in SA patients with isolated erythroid phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903506.RA5cWOMDC_biLSPgbcb8EbahNngKOZRlcRCzWtYMu-45w130_provenance.