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

AuthID
P-000-B1H

Author(s)

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

Document Type

Article

Year published

2004

Published

in JOURNAL OF MEDICAL GENETICS, ISSN: 1468-6244

Volume: 41, Issue: 4, Pages: e51-e51 (5)

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Scopus^®

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Pubmed^®

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Publication Identifiers

DOI: 10.1136/jmg.2003.014803

Pubmed: 15060127

Scopus: 2-s2.0-2342614233

Wos: WOS:000220589100031

Source Identifiers

ISSN: 1468-6244

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

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

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