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Detection of a de novo heterozygous ANK2 variant in a child with autism spectrum disorder and epilepsy: a case report.

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Title: Detection of a de novo heterozygous ANK2 variant in a child with autism spectrum disorder and epilepsy: a case report.
Authors: Morais, Catarina Granjo1 (AUTHOR) catarina.granjo.morais@chsj.min-saude.pt, Quental, Rita2 (AUTHOR), Lourenço, Lara3 (AUTHOR), Guardiano, Micaela3 (AUTHOR), Silva, Cármen3 (AUTHOR), Leão, Miguel2 (AUTHOR)
Source: Egyptian Journal of Medical Human Genetics. 1/21/2023, Vol. 24 Issue 1, p1-4. 4p.
Database: Academic Search Ultimate
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  Data: Detection of a de novo heterozygous ANK2 variant in a child with autism spectrum disorder and epilepsy: a case report.
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  Data: <searchLink fieldCode="AR" term="%22Morais%2C+Catarina+Granjo%22">Morais, Catarina Granjo</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> catarina.granjo.morais@chsj.min-saude.pt</i><br /><searchLink fieldCode="AR" term="%22Quental%2C+Rita%22">Quental, Rita</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lourenço%2C+Lara%22">Lourenço, Lara</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Guardiano%2C+Micaela%22">Guardiano, Micaela</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Silva%2C+Cármen%22">Silva, Cármen</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Leão%2C+Miguel%22">Leão, Miguel</searchLink><relatesTo>2</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Egyptian+Journal+of+Medical+Human+Genetics%22">Egyptian Journal of Medical Human Genetics</searchLink>. 1/21/2023, Vol. 24 Issue 1, p1-4. 4p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=161416441
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1186/s43042-023-00389-y
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      – Code: eng
        Text: English
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        PageCount: 4
        StartPage: 1
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      – TitleFull: Detection of a de novo heterozygous ANK2 variant in a child with autism spectrum disorder and epilepsy: a case report.
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            NameFull: Morais, Catarina Granjo
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            NameFull: Quental, Rita
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            NameFull: Lourenço, Lara
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            NameFull: Guardiano, Micaela
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            NameFull: Silva, Cármen
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            NameFull: Leão, Miguel
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            – D: 21
              M: 01
              Text: 1/21/2023
              Type: published
              Y: 2023
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              Value: 24
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            – TitleFull: Egyptian Journal of Medical Human Genetics
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