Matches in Nanopublications for { ?s ?p "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- NP164040.RAjslgIj9AiQVOsZ8s6zWtccIXRbpOZyPOtay7qwHdLng130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164040.RAjslgIj9AiQVOsZ8s6zWtccIXRbpOZyPOtay7qwHdLng130_provenance.
- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_provenance.
- NP33608.RA1Ri2vaVCsrJwLvJATu44cII81iWWKTLfiBicZEHluLE130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33608.RA1Ri2vaVCsrJwLvJATu44cII81iWWKTLfiBicZEHluLE130_provenance.
- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_provenance.
- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- NP852631.RAFBeQyFkAxezM8Bhz3lEzVUzjkES1lwdkZnoiCq2ksWM130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852631.RAFBeQyFkAxezM8Bhz3lEzVUzjkES1lwdkZnoiCq2ksWM130_provenance.
- NP376876.RA79kVfi3permXliAqWezdWXpRo9JRJ0YA4QNsiYgWBEA130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376876.RA79kVfi3permXliAqWezdWXpRo9JRJ0YA4QNsiYgWBEA130_provenance.
- assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_provenance.
- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_provenance.