http://rdf.ncbi.nlm.nih.gov/pubchem/reference/599326

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contentType Case Reports|Journal Article|Research Support, Non-U.S. Gov't
issn 2324-9269
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publicationName Molecular genetics & genomic medicine
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bibliographicCitation Wang D, Hu D, Guo Z, Hu R, Wang Q, Liu Y, Liu M, Meng Z, Yang H, Zhang Y, Cai F, Zhou W, Song W. A novel de novo nonsense mutation in ZC4H2 causes Wieacker-Wolff Syndrome. Mol Genet Genomic Med. 2020 Feb;8(2):e1100. PMID: 31885220; PMCID: PMC7005642.
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date 2019-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/PMC7005642
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language English
source https://pubmed.ncbi.nlm.nih.gov/
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title A novel de novo nonsense mutation in ZC4H2 causes Wieacker‐Wolff Syndrome
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Total number of triples: 40.