A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene

CHIH-HAO CHENHuang C.-W.MING-JEN LEE2020-11-112020-11-1120140929-6646https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904385293&doi=10.1016%2fj.jfma.2012.07.026&partnerID=40&md5=2a95bc633302c953eb34475b492e0bcfhttps://scholars.lib.ntu.edu.tw/handle/123456789/520725[SDGs]SDG3amyloid; prealbumin; adult; anhidrosis; areflexia; article; autonomic dysfunction; case report; clinical feature; conformational transition; diarrhea; dizziness; erectile dysfunction; familial amyloid polyneuropathy; gene; gene mutation; gene sequence; genetic counseling; genetic screening; human; hyperalgesia; limb weakness; male; middle aged; molecular mimicry; muscle atrophy; nerve conduction; orthostatic hypotension; polyneuropathy; rare disease; restrictive cardiomyopathy; TTR gene; unsteadiness; genetics; mutation; nucleotide sequence; pathology; DNA Mutational Analysis; Humans; Male; Middle Aged; Mutation; Polyneuropathies; PrealbuminA case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR genejournal article10.1016/j.jfma.2012.07.026250377662-s2.0-84904385293