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Genomic analysis identify a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease.

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Title: Genomic analysis identify a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease.
Authors: Cerantonio, Annamaria1 (AUTHOR), De Benedittis, Selene1 (AUTHOR), Muglia, Maria2 (AUTHOR), Spadafora, Patrizia2 (AUTHOR), Cavalcanti, Francesca2 (AUTHOR), Lanza, Pierluigi2 (AUTHOR), Gallo, Olivier2 (AUTHOR), Di Palma, Gemma2 (AUTHOR), Romeo, Nelide3 (AUTHOR), Bagalà, Angelo2 (AUTHOR), Mazzei, Rosalucia3 (AUTHOR), Propato, Flavia4 (AUTHOR), Consoli, Domenico5 (AUTHOR), Cerasa, Antonio2 (AUTHOR), Qualtieri, Antonio2 (AUTHOR), Citrigno, Luigi2 (AUTHOR)
Source: Journal of the Neurological Sciences. 2021 Supplement, Vol. 429, pN.PAG-N.PAG. 1p.
Database: Academic Search Ultimate
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  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 152897730
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: Genomic analysis identify a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease.
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+the+Neurological+Sciences%22">Journal of the Neurological Sciences</searchLink>. 2021 Supplement, Vol. 429, pN.PAG-N.PAG. 1p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=152897730
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      – Type: doi
        Value: 10.1016/j.jns.2021.118284
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      – Code: eng
        Text: English
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        PageCount: 1
        StartPage: N.PAG
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      – TitleFull: Genomic analysis identify a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease.
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              Text: 2021 Supplement
              Type: published
              Y: 2021
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              Value: 429
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