Matches in Nanopublications for { ?s ?p "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP700040.RA6MVNkfW4ejHWedSXarz2NORbajD0PpIVi7wzCLHA344130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700040.RA6MVNkfW4ejHWedSXarz2NORbajD0PpIVi7wzCLHA344130_provenance.
- assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709732.RADb86HVA0sKTcEmrm-lYppYRScVnEBEO5Tufrgo5Zof8130_provenance.
- NP709734.RAYutWxNccZ4WrsJhEBXFf2N-zmxWXGLbvP5_3YEhCjnI130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709734.RAYutWxNccZ4WrsJhEBXFf2N-zmxWXGLbvP5_3YEhCjnI130_provenance.
- NP709733.RAMfdh7iE7IRuwfznV7-a5FERphBJSPuGimaYY7fqET-Y130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709733.RAMfdh7iE7IRuwfznV7-a5FERphBJSPuGimaYY7fqET-Y130_provenance.
- NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910590.RA5bB5ZHnIg4QkOw92pQTSQgGnz2qLOTJloSvQq4h_0ME130_provenance.
- NP910592.RA5f4IRI2_ola0YLMr7xD4TOXGhXmZ5u9zn7NxcRO9fWc130_assertion description "[Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP910592.RA5f4IRI2_ola0YLMr7xD4TOXGhXmZ5u9zn7NxcRO9fWc130_provenance.