reference/17677006

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17677006

Outgoing Links

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bibliographicCitation	Vincent KM, Eaton A, Yassaee VR, Miryounesi M, Hashemi‐Gorji F, Rudichuk L, Goez H, Leonard N, Lazier J. Delineating the expanding phenotype of HERC2‐related disorders: The impact of biallelic loss of function versus missense variation. Clinical Genetics. 2021 Aug 09;100(5):637–40. doi: 10.1111/cge.14039.
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date	2021-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/cge.14039 https://pubmed.ncbi.nlm.nih.gov/34370298
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Delineating the expanding phenotype of HERC2‐related disorders: The impact of biallelic loss of function versus missense variation
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Total number of triples: 47.