Matches in Nanopublications for { ?s ?p "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657262.RACoXEiD9a84WCxQvX9IyW2-MKk3qtivLD9sNUywbWdO4130_provenance.
- NP432591.RA2v7IqhteIQ2bwqF44LzzBTVGIaUHXc2tbjr1HjpEcME130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432591.RA2v7IqhteIQ2bwqF44LzzBTVGIaUHXc2tbjr1HjpEcME130_provenance.
- NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710149.RAbtNcEwtUljXx-19Ll64JYRVZGp41usp3HdPEs6PazUQ130_provenance.
- assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621336.RAM9C9Y1QfW0oTG-FXUGiJWu1yP4rp0l3W_D_oPg3yHEo130_provenance.
- NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710138.RA1krSLVssAYTr3mWprlPRk4_9M35a3nrfluNW8Xe9tkQ130_provenance.
- NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621335.RA4lyC_x_pwdehZaTIWR3Etodb2HMstB9f195EvALSePM130_provenance.