Homozygous Deletion of the Epigenetic Regulator PHF20 in Individuals With Neurodevelopmental Disorder.

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Bibliographic Details
Title: Homozygous Deletion of the Epigenetic Regulator PHF20 in Individuals With Neurodevelopmental Disorder.
Authors: Dagan SY; Department of Genetics, Hadassah Medical Center, Jerusalem, Israel, hadassah.org.il., Xuan H; Department of Epigenetics, Van Andel Institute, Grand Rapids, Michigan, USA, vai.org., Rips J; Department of Genetics, Hadassah Medical Center, Jerusalem, Israel, hadassah.org.il.; Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel, huji.ac.il., Paz-Ebstein E; Department of Genetics, Hadassah Medical Center, Jerusalem, Israel, hadassah.org.il.; Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel, huji.ac.il., Baer T; Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel, huji.ac.il., Gross S; Department of Genetics, Hadassah Medical Center, Jerusalem, Israel, hadassah.org.il.; Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel, huji.ac.il., Frumkin A; Department of Genetics, Hadassah Medical Center, Jerusalem, Israel, hadassah.org.il.; Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel, huji.ac.il., Shi X; Department of Epigenetics, Van Andel Institute, Grand Rapids, Michigan, USA, vai.org., Harel T; Department of Genetics, Hadassah Medical Center, Jerusalem, Israel, hadassah.org.il.; Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel, huji.ac.il.
Source: Human mutation [Hum Mutat] 2025 Dec 22; Vol. 2025, pp. 6484814. Date of Electronic Publication: 2025 Dec 22 (Print Publication: 2025).
Publication Type: Journal Article; Case Reports
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
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