reference/440764

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/440764

Outgoing Links

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endingPage	2053
issn	0964-6906 1460-2083
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pageRange	2039-2053
publicationName	Human Molecular Genetics
startingPage	2039
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bibliographicCitation	Purevjav E, Arimura T, Augustin S, Huby AC, Takagi K, Nunoda S, Kearney DL, Taylor MD, Terasaki F, Bos JM, Ommen SR, Shibata H, Takahashi M, Itoh-Satoh M, McKenna WJ, Murphy RT, Labeit S, Yamanaka Y, Machida N, Park JE, Alexander PM, Weintraub RG, Kitaura Y, Ackerman MJ, Kimura A, Towbin JA. Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. Hum Mol Genet. 2012 May 01;21(9):2039–53. PMID: 22286171; PMCID: PMC3315208.
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date	2012-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC3315208 https://pubmed.ncbi.nlm.nih.gov/22286171 https://doi.org/10.1093/hmg/dds022
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations
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