reference/3961868

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3961868

Outgoing Links

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contentType	Case Reports\|Letter\|Research Support, Non-U.S. Gov't
endingPage	144
issn	0022-510X
pageRange	142-144
publicationName	Journal of the Neurological Sciences
startingPage	142
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_2deed1e38cd8a78ccf991074a7d2443a http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_69ab79955a9fb86a2eff0e11c7e44e24 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_182d91f897e6a049bb202e2488ad0ed4 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_bbd74ac275fb198d0d8265b6ba158b91 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_0ef50675734f54de7f89007bfc13219e
bibliographicCitation	Tadokoro K, Ohta Y, Sasaki R, Takahashi Y, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, Nakamura K, Nishino I, Abe K. Congenital myopathy with fiber-type disproportion accompanied by dilated cardiomyopathy in a patient with a novel p.G48A ACTA1 mutation. Journal of the Neurological Sciences. 2018 Oct;393():142–4. doi: 10.1016/j.jns.2018.08.015.
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date	2018-10-15^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/30195123 https://doi.org/10.1016/j.jns.2018.08.015
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5010 https://portal.issn.org/resource/ISSN/0022-510X
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Congenital myopathy with fiber-type disproportion accompanied by dilated cardiomyopathy in a patient with a novel p.G48A ACTA1 mutation
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