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Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder.

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Title: Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder.
Authors: Liaqat K; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA., Treat K; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA., Wilson TE; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Conboy E; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA., Vetrini F; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA.
Source: Clinical genetics [Clin Genet] 2024 Apr; Vol. 105 (4), pp. 455-456. Date of Electronic Publication: 2024 Feb 12.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder.
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  Data: <searchLink fieldCode="AU" term="%22Liaqat+K%22">Liaqat K</searchLink>; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA.<br /><searchLink fieldCode="AU" term="%22Treat+K%22">Treat K</searchLink>; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA.<br /><searchLink fieldCode="AU" term="%22Wilson+TE%22">Wilson TE</searchLink>; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.<br /><searchLink fieldCode="AU" term="%22Conboy+E%22">Conboy E</searchLink>; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA.<br /><searchLink fieldCode="AU" term="%22Vetrini+F%22">Vetrini F</searchLink>; Department of Medical and Molecular Genetics, Undiagnosed Rare Disease Clinic (URDC), Indiana University School of Medicine, Indianapolis, Indiana, USA.
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  Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2024 Apr; Vol. 105 (4), pp. 455-456. <i>Date of Electronic Publication: </i>2024 Feb 12.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1111/cge.14497
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      – Code: eng
        Text: English
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      – TitleFull: Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder.
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            NameFull: Liaqat K
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            NameFull: Treat K
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            NameFull: Wilson TE
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              M: 04
              Text: 2024 Apr
              Type: published
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