http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5425546

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contentType Journal Article|Research Support, Non-U.S. Gov't|Review
issn 1750-1172
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pageRange 467-
publicationName Orphanet Journal of Rare Diseases
startingPage 467
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bibliographicCitation Zhang W, Sang Y. Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism. Orphanet Journal of Rare Diseases. 2021 Nov 04;16(1):467. doi: 10.1186/s13023-021-02088-6.
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date 2021-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/34736508
https://pubmed.ncbi.nlm.nih.gov/PMC8567654
https://doi.org/10.1186/s13023-021-02088-6
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language English
source https://scigraph.springernature.com/
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism
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Total number of triples: 30.