reference/12945503

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publicationName	American journal of medical genetics. Part A
startingPage	2526
bibliographicCitation	Brunetti S, Malerba L, Giordano L, Parrini E, Guerrini R, Palumbo G, Parazzini C, Bestetti I, Accorsi P. Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene. American J of Med Genetics Pt A. 2021 May 19;185(8):2526–31. doi: 10.1002/ajmg.a.62345.
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date	2021-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ajmg.a.62345 https://pubmed.ncbi.nlm.nih.gov/34008900
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene
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