reference/7524259

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7524259

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
issn	1750-1172
issueIdentifier	1
pageRange	411-
publicationName	Orphanet Journal of Rare Diseases
startingPage	411
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bibliographicCitation	Adams D, Algalarrondo V, Polydefkis M, Sarswat N, Slama MS, Nativi-Nicolau J. Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression. Orphanet Journal of Rare Diseases. 2021 Oct 03;16(1):411. doi: 10.1186/s13023-021-01960-9.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7823c8b4470dcfcc6db8ab6aa78df21b http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-5481-2122 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_eb6a72ad4fcd6fe53305f2d0fd2ae1dc http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5d7476524a2ef7131ec5b1c9e8a5d191 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_02d6270707e6c07af2404ddc6fc63a1f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f3c312b54f9197d3c28bec4a200a29fc
date	2021-10-03^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC8489116 https://doi.org/10.1186/s13023-021-01960-9 https://pubmed.ncbi.nlm.nih.gov/34602081
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32787 https://portal.issn.org/resource/ISSN/1750-1172
language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression
discusses	http://id.nlm.nih.gov/mesh/M0017446
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