Matches in Nanopublications for { ?s ?p "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP607.RAUkxUHT6_Bn73boE6srxmxB0QqsU6VTRcsYpRe1ieTsQ130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607.RAUkxUHT6_Bn73boE6srxmxB0QqsU6VTRcsYpRe1ieTsQ130_provenance.
- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_provenance.
- NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718520.RA34JVB8UQa572dW-QN1h87hOiL2wKJCaJk0cMJbrk2Nw130_provenance.
- NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5670.RAR4THIyOIBPpbe8qcHkSP5FbZyituM8HTZBpkQywTdEg130_provenance.
- assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_provenance.