TY - JOUR T1 - Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. JF - Journal of medical genetics Y1 - 2004 A1 - Ohmori, H. A1 - Ando, Y. A1 - Makita, Y. A1 - Onouchi, Y. A1 - Nakajima, T. A1 - Saraiva, M.J. A1 - Terazaki, H. A1 - Suhr, O. A1 - Sobue, G. A1 - Nakamura, M. A1 - Yamaizumi, M. A1 - Munar-Ques, M. A1 - Inoue, I. A1 - Uchino, M. A1 - Hata, A. VL - 41 UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-2342614233&partnerID=40&md5=fb2e8747448af9b1e28fcf2650bb3b32 IS - 4 N1 - Cited By (since 1996): 16Export Date: 18 March 2013Source: Scopus ER -