Matches in Nanopublications for { ?s ?p "[Point mutations in SPG4, the gene encoding spastin, are a frequent cause of autosomal dominant hereditary spastic paraplegia (AD-HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_assertion description "[Point mutations in SPG4, the gene encoding spastin, are a frequent cause of autosomal dominant hereditary spastic paraplegia (AD-HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257082.RAdi7ie7AUIgGn8fYwqcBUZUEKUjhcj3fu-zO_EKlMCqc130_provenance.