reference/23750243

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publicationName	American journal of medical genetics. Part A
startingPage	3092
bibliographicCitation	Ueda K, Ogawa S, Matsuda K, Hasegawa Y, Nishi E, Yanagi K, Kaname T, Yamamoto T, Okamoto N. Blended phenotype of combination of HERC2 and AP3B2 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15. American J of Med Genetics Pt A. 2021 May 27;185(10):3092–8. doi: 10.1002/ajmg.a.62371.
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date	2021-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/34042275 https://doi.org/10.1002/ajmg.a.62371
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Blended phenotype of combination of HERC2 and AP3B2 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15
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