Common Origin of the Val30Met Mutation Responsible for the Amyloidogenic Transthyretin Type of Familial Amyloidotic Polyneuropathy

AuthID
 P-000-B1H
15
Author(s)
Ando, Y
·
Nakajima, T
·
Terazaki, H
·
Suhr, O
·
Nakamura, M
·
Yamaizumi, M
·
Munar Ques, M
·
Inoue, I
·
Uchino, M
·
Hata, A
Document Type
Article
Year published
2004
Published
in JOURNAL OF MEDICAL GENETICS, ISSN: 1468-6244
Volume: 41, Issue: 4, Pages: e51-e51 (5)
Indexing
Wos®
Scopus®
Crossref®42
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 15060127
Scopus: 2-s2.0-2342614233
Wos: WOS:000220589100031
Source Identifiers
ISSN: 1468-6244
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