Predicate |
Object |
contentType |
Journal Article|Research Support, N.I.H., Extramural |
endingPage |
1013 |
issn |
0022-2828 |
issueIdentifier |
5 |
pageRange |
1007-1013 |
publicationName |
Journal of molecular and cellular cardiology |
startingPage |
1007 |
hasFundingAgency |
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bibliographicCitation |
Armel TZ, Leinwand LA. Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes. Journal of Molecular and Cellular Cardiology. 2010 May;48(5):1007–13. doi: 10.1016/j.yjmcc.2009.10.011. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3d4fbfa5ecfa3c39a6823d2e89b62b33 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_52e4b7a0e349d2987d33d39348ee243a |
date |
201005 |
identifier |
https://pubmed.ncbi.nlm.nih.gov/19854198 https://doi.org/10.1016/j.yjmcc.2009.10.011 https://pubmed.ncbi.nlm.nih.gov/PMC2854248 |
isPartOf |
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4968 https://portal.issn.org/resource/ISSN/0022-2828 |
language |
English |
source |
https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ |
title |
Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes |
discusses |
http://id.nlm.nih.gov/mesh/M0000922 http://id.nlm.nih.gov/mesh/M0024319 http://id.nlm.nih.gov/mesh/M0014361 |
discussesAsDerivedByTextMining |
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