reference/24452369

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24452369

Outgoing Links

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publicationName	Molecular Genetics & Genomic Medicine
startingPage	e1912
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bibliographicCitation	Lau K, Üçeyler N, Cairns T, Lorenz L, Sommer C, Schindehütte M, Amann K, Wanner C, Nordbeck P. Gene variants of unknown significance in Fabry disease: Clinical characteristics of c.376A>G (p.Ser126Gly). Mol Genet Genomic Med. 2022 May;10(5):e1912. PMID: 35212486; PMCID: PMC9034661.
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date	2022-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC9034661 https://pubmed.ncbi.nlm.nih.gov/35212486 https://doi.org/10.1002/mgg3.1912
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Gene variants of unknown significance in Fabry disease: Clinical characteristics of c.376A>G (p.Ser126Gly)
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Incoming Links

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Total number of triples: 44.