Matches in Nanopublications for { ?s ?p "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP184755.RAalZHymJYpuZfBHGHXRMezLenWinLmntvyK3SbjdKAkg130_assertion description "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184755.RAalZHymJYpuZfBHGHXRMezLenWinLmntvyK3SbjdKAkg130_provenance.
- NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_assertion description "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184756.RASQgLjV1gcLK47zXat7wAZpX_SkxQO2-_u5TZUryI1_M130_provenance.
- NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_assertion description "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158934.RAxQZWAMWOrcjIYhI829GK0m1oxgOw_UUhFw7tj8J4ZXE130_provenance.
- NP126848.RAGeJ_jBM0YjD6AVk_fGLswM1UBGzH8RnIP0bfVUFlGlw130_assertion description "[The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126848.RAGeJ_jBM0YjD6AVk_fGLswM1UBGzH8RnIP0bfVUFlGlw130_provenance.