Matches in Nanopublications for { ?s ?p "[The Finnish type of familial amyloid polyneuropathy (FAF) is an autosomal dominant form of systemic amyloidosis caused by a mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP663649.RArMfus359BJHk_uNMOKkY1r5nIUP1ICZW-n4MPD-HBr4130_assertion description "[The Finnish type of familial amyloid polyneuropathy (FAF) is an autosomal dominant form of systemic amyloidosis caused by a mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663649.RArMfus359BJHk_uNMOKkY1r5nIUP1ICZW-n4MPD-HBr4130_provenance.
- NP436855.RAfdWojouifbpuJoslTONyI_B0vEhkFhGMFu0VQJRk-hk130_assertion description "[The Finnish type of familial amyloid polyneuropathy (FAF) is an autosomal dominant form of systemic amyloidosis caused by a mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436855.RAfdWojouifbpuJoslTONyI_B0vEhkFhGMFu0VQJRk-hk130_provenance.
- NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_assertion description "[The Finnish type of familial amyloid polyneuropathy (FAF) is an autosomal dominant form of systemic amyloidosis caused by a mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409873.RAbIyvZaAOJRn1_7LbJfzTq1f5ePXlQ6qR9hDNS5tVWsU130_provenance.