reference/1046015

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1046015

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endingPage	587
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publicationName	Clinical Genetics
startingPage	585
bibliographicCitation	Ramos-Arroyo MA, Hualde J, Ayechu A, De Meirleir L, Seneca S, Nadal N, Briones P. Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene. Clin Genet. 2009 Jun;75(6):585–7. doi: 10.1111/j.1399-0004.2009.01160.x. PMID: 19508421.
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date	200906
identifier	https://doi.org/10.1111/j.1399-0004.2009.01160.x https://pubmed.ncbi.nlm.nih.gov/19508421
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene
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Total number of triples: 51.