reference/26866347

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26866347

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bibliographicCitation	Smith BN, Bevan S, Vance C, Renwick P, Wilkinson P, Proukakis C, Squitieri F, Berardelli A, Warner TT, Reid E, Shaw CE. Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype. Clin Genet. 2009 May;75(5):485–9. doi: 10.1111/j.1399-0004.2009.01184.x. PMID: 19459885.
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date	2009-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra‐familial variability in age of onset and complex phenotype
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