H. Ohmori
AuthID: R-00H-8VG
1
TITLE: Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy
AUTHORS: Ohmori, H; Ando, Y; Makita, Y; Onouchi, Y; Nakajima, T; Saraiva, MJM ; Terazaki, H; Suhr, O; Sobue, G; Nakamura, M; Yamaizumi, M; Munar Ques, M; Inoue, I; Uchino, M; Hata, A;
PUBLISHED: 2004, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 41, ISSUE: 4
AUTHORS: Ohmori, H; Ando, Y; Makita, Y; Onouchi, Y; Nakajima, T; Saraiva, MJM ; Terazaki, H; Suhr, O; Sobue, G; Nakamura, M; Yamaizumi, M; Munar Ques, M; Inoue, I; Uchino, M; Hata, A;
PUBLISHED: 2004, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 41, ISSUE: 4
