Matches in Nanopublications for { ?s ?p "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP792335.RAUTfzkstReKU908Z2F9xXxwX_EjDz4fJeRQNsYMJOJO0130_assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792335.RAUTfzkstReKU908Z2F9xXxwX_EjDz4fJeRQNsYMJOJO0130_provenance.
- assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1117077.RAcAxAqIfKdqtL_Sk7nDeW5tG5t3n6VCgHfSKG_XGMK2A130_assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117077.RAcAxAqIfKdqtL_Sk7nDeW5tG5t3n6VCgHfSKG_XGMK2A130_provenance.
- assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP963737.RArU4T_oDL4MCm3iaWe3VdqrGqqA4JI-O5FmEYC3_A29I130_assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963737.RArU4T_oDL4MCm3iaWe3VdqrGqqA4JI-O5FmEYC3_A29I130_provenance.
- NP1117076.RAG_O5Wx1GWmMKvIVMekfc-6SQdvR-6fUcN8XoHm-5JVw130_assertion description "[Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients with benign (familial) infantile convulsions (B(F)IC), infantile convulsions with choreoathetosis (ICCA) and paroxysmal dyskinesias (PDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117076.RAG_O5Wx1GWmMKvIVMekfc-6SQdvR-6fUcN8XoHm-5JVw130_provenance.