reference/11560921

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11560921

Outgoing Links

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contentType	Letter\|Research Support, Non-U.S. Gov't\|Comment
endingPage	1004
issn	2328-9503
issueIdentifier	4
pageRange	1002-1004
publicationName	Annals of Clinical and Translational Neurology
startingPage	1002
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bibliographicCitation	Yau WY, Chen Z, Sullivan R, Vandrovcova J, Houlden H. Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant? Ann Clin Transl Neurol. 2021 Apr;8(4):1002–4. PMID: 33780167; PMCID: PMC8045916.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6284-9163 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1938b57f6ab3a78d2def0a72696dc4f9 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-4636-8033 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6668-7202 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2d7689f5e8ec1210977d97cd8a87f472
date	2021-03-29^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/acn3.51330 https://pubmed.ncbi.nlm.nih.gov/PMC8045916 https://pubmed.ncbi.nlm.nih.gov/33780167
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant?
discusses	http://id.nlm.nih.gov/mesh/C537395
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D018740 http://id.nlm.nih.gov/mesh/D019636Q000235
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D045586

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