Matches in Nanopublications for { ?s ?p "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485622.RADpjysbG71vgZ8ktTwjnDhyR8hV-mvj7_7pc4xD3CqQs130_provenance.
- NP601567.RADCw3iyPNKx7BUmW7JIiuCLwUHQdRU3oyKbCMmWXmMq0130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601567.RADCw3iyPNKx7BUmW7JIiuCLwUHQdRU3oyKbCMmWXmMq0130_provenance.
- NP668656.RAvviYC8j0VKlFyJXWxyH3BfK8cvYidDismUGef4B-ARs130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668656.RAvviYC8j0VKlFyJXWxyH3BfK8cvYidDismUGef4B-ARs130_provenance.
- NP781217.RAb4oFnrii7dvKKSmmtPpopdbIxA-NRYpnV-0J0mpZFc8130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781217.RAb4oFnrii7dvKKSmmtPpopdbIxA-NRYpnV-0J0mpZFc8130_provenance.
- NP870216.RAXp_c0rfu7wzg-ZAqk4BPYPDVO2PcMf5EhbnvMA4h6Tg130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870216.RAXp_c0rfu7wzg-ZAqk4BPYPDVO2PcMf5EhbnvMA4h6Tg130_provenance.
- assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623351.RASNTqy1wDakDpnvaYyeiNmwYKNPwBZQM3MHF5d9tgu0Q130_provenance.
- NP623353.RAmTYaCot5lbVJS4AQG-qlCEykSgaVUzkRS1NWP0Lg1q0130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623353.RAmTYaCot5lbVJS4AQG-qlCEykSgaVUzkRS1NWP0Lg1q0130_provenance.
- NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_assertion description "[Chorea-acanthocytosis (ChAc) is an autosomal recessive hereditary disease characterized by neurodegeneration in the striatum and acanthocytosis that is caused by mutations in the VPS13A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870162.RA-B8cyF-eAc0rY2N3YLXBZygkPMI1ZS1obxXPnxy40lU130_provenance.