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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ISSN:1399-0004
DOI:10.1111/cge.14497