Matches in Nanopublications for { ?s ?p "[Patients with congenital presynaptic failure, including two patients with episodic ataxia type 2 (EA-2) due to CACNA1A mutations, were studied with muscle biopsy, microelectrode studies, electron microscopy, DNA amplification, and sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP418873.RAB4VTKw4i4KLm-mwELkd10-cJKXf4sE2lkTmciBNrM5Y130_assertion description "[Patients with congenital presynaptic failure, including two patients with episodic ataxia type 2 (EA-2) due to CACNA1A mutations, were studied with muscle biopsy, microelectrode studies, electron microscopy, DNA amplification, and sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418873.RAB4VTKw4i4KLm-mwELkd10-cJKXf4sE2lkTmciBNrM5Y130_provenance.