@article{c490f111a1c14c93b9702e7915210e5a,
title = "Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: A cohort study in Ontario, Canada",
keywords = "Health service utilization, Inherited metabolic diseases, Medium-chain acyl-CoA dehydrogenase deficiency, Newborn screening",
author = "Karaceper, {Maria D.} and Khangura, {Sara D.} and Kumanan Wilson and Doug Coyle and Marni Brownell and Christine Davies and Linda Dodds and Annette Feigenbaum and Fell, {Deshayne B.} and Grosse, {Scott D.} and Astrid Guttmann and Steven Hawken and Hayeems, {Robin Z.} and Kronick, {Jonathan B.} and Laberge, {Anne Marie} and Julian Little and Aizeddin Mhanni and Mitchell, {John J.} and Meranda Nakhla and Murray Potter and Chitra Prasad and Cheryl Rockman-Greenberg and Rebecca Sparkes and Sylvia Stockler and Keiko Ueda and Hilary Vallance and Wilson, {Brenda J.} and Pranesh Chakraborty and Potter, {Beth K.}",
note = "Publisher Copyright: {\textcopyright} 2019 The Author(s).",
year = "2019",
month = mar,
day = "22",
doi = "10.1186/s13023-019-1001-0",
language = "English",
volume = "14",
journal = "Orphanet Journal of Rare Diseases",
issn = "1750-1172",
publisher = "BioMed Central",
number = "1",
}