Matches in Nanopublications for { ?s ?p "[The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand beyond the distinct yet overlapping phenotypes in patients with AHC, RDP, and CAPOS syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_assertion description "[The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand beyond the distinct yet overlapping phenotypes in patients with AHC, RDP, and CAPOS syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242287.RA6SirmDEX3dYV4SA84EBCJwk_e-WSzBDoKzPwghT0iic130_provenance.
- NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_assertion description "[The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand beyond the distinct yet overlapping phenotypes in patients with AHC, RDP, and CAPOS syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242288.RA7qUrJ9RQ2o63cKBD_-xLX-3ung25Cqf066KwRtaCNXk130_provenance.
- NP1242289.RA3Lw76URuseUO1iNbsct37PYaWzbnP8XHdTrqZr21qlE130_assertion description "[The phenotypic spectrum of ATP1A3-related neurological disorders continues to expand beyond the distinct yet overlapping phenotypes in patients with AHC, RDP, and CAPOS syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242289.RA3Lw76URuseUO1iNbsct37PYaWzbnP8XHdTrqZr21qlE130_provenance.