Journal ID (nlm-ta): Orphanet J Rare Dis
Journal ID (iso-abbrev): Orphanet J Rare Dis
Title:
Orphanet Journal of Rare Diseases
Publisher:
BioMed Central
ISSN
(Electronic):
1750-1172
Publication date Collection: 2015
Publication date
(Electronic):
2
November
2015
Volume: 10
Issue: Suppl 1
Page: P11
Affiliations
[1
]Pfizer, Global Innovative Products, NY 10017, New York, USA
[2
]Pfizer, Global Innovative Products-Statistics, CT 06340, Groton, USA
[3
]inVentiv Health, Statistician, MA 01803, Burlington, USA
[4
]Pfizer, Specialty Care Medicines Development Group, CT 06340, Groton, USA
[5
]Pfizer, Global Innovative Pharma Business, PA 19426, Collegeville, USA
Article
Publisher ID:
1750-1172-10-S1-P11
DOI: 10.1186/1750-1172-10-S1-P11
PMC ID: 4642035
SO-VID: 87e1d77b-d277-49cc-8ae0-384eabaa6ba0
Copyright © Copyright © 2015 Keohane et al.
License:
This is an Open Access article distributed under the terms of the Creative Commons
Attribution License (
http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided
the original work is properly cited. The Creative Commons Public Domain Dedication
waiver (
http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Conference name:
First European Congress on Hereditary ATTR amlyoidosis
Conference location:
Paris, France
Conference date:
2-3 November 2015