Matches in Nanopublications for { ?s ?p "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629186.RAo2QoJFjk0QGMY_UidLKX30I1xQB8fAa1F476h9biGWo130_provenance.
- NP582290.RAcffgC4lU5UzP0kv8vnSiYMFhLyjYxfq61JwNmttzOw8130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582290.RAcffgC4lU5UzP0kv8vnSiYMFhLyjYxfq61JwNmttzOw8130_provenance.
- NP747251.RAwX170dR0ZLL4ZNtsT2kzCzO66a-jTwWQGobzmcrUIZQ130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747251.RAwX170dR0ZLL4ZNtsT2kzCzO66a-jTwWQGobzmcrUIZQ130_provenance.
- NP762643.RASYuCul5H51rhgED8X4d8Pr7kwcolETWZIE5TEOTkpp0130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762643.RASYuCul5H51rhgED8X4d8Pr7kwcolETWZIE5TEOTkpp0130_provenance.
- NP978214.RApvkNRRm0-trozE2tONwZna_LnqUScaUMUrKgh2kaZ1s130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978214.RApvkNRRm0-trozE2tONwZna_LnqUScaUMUrKgh2kaZ1s130_provenance.
- NP835566.RAuELNwimiNwM7A8O19NtYbNNx4FrzNYMEb6kKgB8l7XA130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835566.RAuELNwimiNwM7A8O19NtYbNNx4FrzNYMEb6kKgB8l7XA130_provenance.
- NP762644.RAx8L9NuC2HbGwGmJAKgAKjvSWHRtWZRpM7KKBJXZKS0Y130_assertion description "[We report a new neurodegenerative phenotype associated with a known ARX mutation and causing early abnormal neurodevelopment, a complex movement disorder, and early infantile epileptic encephalopathy with a suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762644.RAx8L9NuC2HbGwGmJAKgAKjvSWHRtWZRpM7KKBJXZKS0Y130_provenance.