Matches in Nanopublications for { ?s ?p "[Purpose: PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP239342.RAq-eIUqDzsn1Iex0osEnlgbFtQeaQAe7W1c-cB91YJAc130_assertion description "[Purpose: PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239342.RAq-eIUqDzsn1Iex0osEnlgbFtQeaQAe7W1c-cB91YJAc130_provenance.
- NP515313.RAgYvK8Ws7egIERLupeM07FaxTqPkomQfLyix827Ycj20130_assertion description "[Purpose: PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP515313.RAgYvK8Ws7egIERLupeM07FaxTqPkomQfLyix827Ycj20130_provenance.
- NP532746.RANBo8Kj_WCsoyhG87ZIEslvDehpxCDJJpGV1F7_ehDmk130_assertion description "[Purpose: PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532746.RANBo8Kj_WCsoyhG87ZIEslvDehpxCDJJpGV1F7_ehDmk130_provenance.
- NP575147.RAHy4uq7eHR5VFYD0v0R-pk4nYul9FAu9khWu9YyL1Slk130_assertion description "[Purpose: PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal epilepsy (BFNE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575147.RAHy4uq7eHR5VFYD0v0R-pk4nYul9FAu9khWu9YyL1Slk130_provenance.