reference/6628055

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6628055

Outgoing Links

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publicationName	BMC Neurology
startingPage	29
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bibliographicCitation	Toro C, Olivé M, Dalakas MC, Sivakumar K, Bilbao JM, Tyndel F, Vidal N, Farrero E, Sambuughin N, Goldfarb LG. Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins. BMC Neurol. 2013 Mar 20;13():29. PMID: 23514108; PMCID: PMC3610280.
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date	2013-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1186/1471-2377-13-29 https://pubmed.ncbi.nlm.nih.gov/PMC3610280 https://pubmed.ncbi.nlm.nih.gov/23514108
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins
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Total number of triples: 46.