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11. A Swedish family with the rare Phe33Leu transthyretin mutation. Holmgren G; Hellman U; Jonasson J; Lundgren HE; Westermark P; Suhr OB Amyloid; 2005 Sep; 12(3):189-92. PubMed ID: 16194875 [TBL] [Abstract][Full Text] [Related]
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17. Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. Ohmori H; Ando Y; Makita Y; Onouchi Y; Nakajima T; Saraiva MJ; Terazaki H; Suhr O; Sobue G; Nakamura M; Yamaizumi M; Munar-Ques M; Inoue I; Uchino M; Hata A J Med Genet; 2004 Apr; 41(4):e51. PubMed ID: 15060127 [No Abstract] [Full Text] [Related]
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