Matches in Nanopublications for { ?s ?p "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.We report mapping of the TRS locus to chromosome 13q12.3 and identify a frameshift mutation in SPG20, encoding spartin ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP141640.RAlUSN475F3XtuRIEe6t6nhFIjFzkECoHjRftbut9u0J8130_assertion description "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.We report mapping of the TRS locus to chromosome 13q12.3 and identify a frameshift mutation in SPG20, encoding spartin ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141640.RAlUSN475F3XtuRIEe6t6nhFIjFzkECoHjRftbut9u0J8130_provenance.
- NP195469.RAKtj4_LlVTWXyhI0Xcc01ll4eyRMC0MBTGrM6-lnykeQ130_assertion description "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.We report mapping of the TRS locus to chromosome 13q12.3 and identify a frameshift mutation in SPG20, encoding spartin ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195469.RAKtj4_LlVTWXyhI0Xcc01ll4eyRMC0MBTGrM6-lnykeQ130_provenance.