Matches in Nanopublications for { ?s ?p "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634976.RAaQw-MnradUE3xuIosdhv0_CWoOJIrrA7Ol4r3l6fkW8130_provenance.
- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_provenance.
- NP695406.RAAfVZCOGMZzi6gCUIt8TNYtqZ1iBcYdOMyJW6fXslYAE130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695406.RAAfVZCOGMZzi6gCUIt8TNYtqZ1iBcYdOMyJW6fXslYAE130_provenance.
- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_provenance.
- NP713672.RADKZ_99RJMOPw09omePXA2qGra5v2bfKMeAwZZO9UKkc130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713672.RADKZ_99RJMOPw09omePXA2qGra5v2bfKMeAwZZO9UKkc130_provenance.
- NP713670.RA047XriXc4tFkIfCRJ2t5W5emIf5EHUmi4TxL4LrLU84130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713670.RA047XriXc4tFkIfCRJ2t5W5emIf5EHUmi4TxL4LrLU84130_provenance.
- NP713668.RAZ-QhI9SWnaKhFDvDfk6yqC5bq9m3elQsoDGbxmMn6jo130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713668.RAZ-QhI9SWnaKhFDvDfk6yqC5bq9m3elQsoDGbxmMn6jo130_provenance.
- assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP695395.RApTYfKvgVZRUrXSEO1z0jjaVBiM5YgaI_RbhhUoL0bG0130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695395.RApTYfKvgVZRUrXSEO1z0jjaVBiM5YgaI_RbhhUoL0bG0130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.