Matches in Nanopublications for { ?s ?p "[Mutations in the receptor expression enhancing protein 1 (REEP1) gene have recently been reported to be associated with an autosomal dominant HSP phenotype (SPG31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in the receptor expression enhancing protein 1 (REEP1) gene have recently been reported to be associated with an autosomal dominant HSP phenotype (SPG31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP940647.RAC2_Yryi8jCLjjjwRYLuOUk0BsMWmeGcaPtGzTdSLRy4130_assertion description "[Mutations in the receptor expression enhancing protein 1 (REEP1) gene have recently been reported to be associated with an autosomal dominant HSP phenotype (SPG31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940647.RAC2_Yryi8jCLjjjwRYLuOUk0BsMWmeGcaPtGzTdSLRy4130_provenance.
- NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_assertion description "[Mutations in the receptor expression enhancing protein 1 (REEP1) gene have recently been reported to be associated with an autosomal dominant HSP phenotype (SPG31).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705779.RA-ODnOO6er3Qu4qhKnW4_BVgXPUj4LDEaWm_2qOJDGtE130_provenance.