Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. Issue 4 (1st April 2004)

Record Type:: Journal Article
Title:: Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. Issue 4 (1st April 2004)
Main 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, M J M
Terazaki, H
Suhr, O
Sobue, G
Nakamura, M
Yamaizumi, M
Munar-Ques, M
Inoue, I
Uchino, M
Hata, A
Abstract:
Is Part Of:: Journal of medical genetics. Volume 41:Issue 4(2004)
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 4(2004)
Issue Display:: Volume 41, Issue 4 (2004)
Year:: 2004
Volume:: 41
Issue:: 4
Issue Sort Value:: 2004-0041-0004-0000
Page Start:: e51
Page End:: e51
Publication Date:: 2004-04-01
Subjects:: familial amyloidotic polyneuropathy -- founder -- haplotype
FAP, familial amyloidotic polyneuropathy -- SNPs, single nucleotide polymorphisms -- TTR, transthyretin
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.2003.014803 ↗
Languages:: English
ISSNs:: 1468-6244
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 18354.xml