Matches in Nanopublications for { ?s ?p "[Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP2993.RAemsctlfsCGfAFvaiAFBckqio4Igf2OFFHw7vKQHeu2w130_assertion description "[Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2993.RAemsctlfsCGfAFvaiAFBckqio4Igf2OFFHw7vKQHeu2w130_provenance.
- assertion description "[Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP3055.RAVzLS7aSwRIZ3tcoJl2qo1xb2rESydaVpUNWR5B_6bBI130_assertion description "[Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3055.RAVzLS7aSwRIZ3tcoJl2qo1xb2rESydaVpUNWR5B_6bBI130_provenance.