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A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy.

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Title: A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy.
Authors: Brugger, Melanie1 (AUTHOR), Becker‐Dettling, Fiona2 (AUTHOR), Brunet, Theresa1 (AUTHOR), Strom, Tim1 (AUTHOR), Meitinger, Thomas1 (AUTHOR), Lurz, Eberhard3 (AUTHOR), Borggraefe, Ingo2,4 (AUTHOR), Wagner, Matias1,5 (AUTHOR) matias.wagner@mri.tum.de
Source: Annals of Clinical & Translational Neurology. Jan2021, Vol. 8 Issue 1, p278-283. 6p.
Database: Academic Search Ultimate
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An: 148229850
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  Data: A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy.
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Clinical+%26+Translational+Neurology%22">Annals of Clinical & Translational Neurology</searchLink>. Jan2021, Vol. 8 Issue 1, p278-283. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=148229850
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1002/acn3.51260
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      – Code: eng
        Text: English
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      Pagination:
        PageCount: 6
        StartPage: 278
    Titles:
      – TitleFull: A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy.
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          Name:
            NameFull: Brugger, Melanie
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            NameFull: Becker‐Dettling, Fiona
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            NameFull: Brunet, Theresa
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            NameFull: Strom, Tim
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            NameFull: Meitinger, Thomas
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            NameFull: Lurz, Eberhard
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            NameFull: Borggraefe, Ingo
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            NameFull: Wagner, Matias
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            – D: 01
              M: 01
              Text: Jan2021
              Type: published
              Y: 2021
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              Value: 8
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              Value: 1
          Titles:
            – TitleFull: Annals of Clinical & Translational Neurology
              Type: main
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