reference/9472385

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9472385

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bibliographicCitation	Danis D, Brennerova K, Skopkova M, Kurdiova T, Ukropec J, Stanik J, Kolnikova M, Gasperikova D. Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients. Endocr Regul. 2018 Apr 01;52(2):110–8. doi: 10.2478/enr-2018-0013. PMID: 29715184.
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date	2018-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.2478/enr-2018-0013 https://pubmed.ncbi.nlm.nih.gov/29715184
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients
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Total number of triples: 56.