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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152271.RA6ebeqR3a1Ou0h0_9emSw8IJUKvt2W_y_K0G39DtagwA130_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.]. 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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215383.RAju_nmVTe_5GOrBHjTH0-fC6BXT_FH7b9G12IbZ1tom8130_provenance.
- NP227458.RAVvfN_hHl5Az9KiE300n4LPvHp3l4d6159W21pW_EvME130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227458.RAVvfN_hHl5Az9KiE300n4LPvHp3l4d6159W21pW_EvME130_provenance.
- NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227457.RAg-v8ucW0NjDdqgFydGRZCVOyWgCnJH9FyszCF9yZSXY130_provenance.
- NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_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.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204777.RAxRd5j2OC-8v7SZMdsEwMnJ6yFI2wmr52weTic5VqKgA130_provenance.