reference/30469017

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30469017

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publicationName	BMC Medical Genetics
startingPage	61
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bibliographicCitation	Sümegi A, Hendrik Z, Gáll T, Felszeghy E, Szakszon K, Antal-Szalmás P, Beke L, Papp Á, Méhes G, Balla J, Balla G. A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary. BMC Medical Genomics. 2020 Mar 27;21(1):61. doi: 10.1186/s12881-020-0985-6.
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date	2020-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1186/s12881-020-0985-6 https://pubmed.ncbi.nlm.nih.gov/PMC7099831 https://pubmed.ncbi.nlm.nih.gov/32216767
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language	English
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title	A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary
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