Matches in Nanopublications for { ?s ?p "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_assertion description "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232250.RAD1b_5rklOZL66BQv0kdtMeTD6emeisX64fhKhCsojcc130_provenance.
- NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_assertion description "[Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232260.RAs1gcU8y8Y4IL_M3Sj4UWtVVVUJmfSux918qdWyaw-D0130_provenance.