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TRMT10A-Related Neurodevelopmental Disorder Without Metabolic Findings.

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Title: TRMT10A-Related Neurodevelopmental Disorder Without Metabolic Findings.
Authors: Ülker Üstebay D; Department of Pediatric Neurology, Faculty of Medicine, Bandırma Onyedi Eylül University, Balıkesir, Türkiye, bandirma.edu.tr., Aksu Şahin İ; Department of Medical Genetics, Faculty of Medicine, Balıkesir University, Balıkesir, Türkiye, balikesir.edu.tr., Üstebay S; Department of Pediatrics, Faculty of Medicine, Bandırma Onyedi Eylül University, Bandırma, Türkiye, bandirma.edu.tr., Ünsel Bolat G; Department of Child and Adolescent Psychiatry, Faculty of Medicine, Balıkesir University, Balıkesir, Türkiye, balikesir.edu.tr., Bolat H; Department of Medical Genetics, Faculty of Medicine, Balıkesir University, Balıkesir, Türkiye, balikesir.edu.tr.
Source: Human mutation [Hum Mutat] 2026 May 22; Vol. 2026, pp. 8058409. Date of Electronic Publication: 2026 May 22 (Print Publication: 2026).
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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  Data: TRMT10A-Related Neurodevelopmental Disorder Without Metabolic Findings.
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  Data: <searchLink fieldCode="AU" term="%22Ülker+Üstebay+D%22">Ülker Üstebay D</searchLink>; Department of Pediatric Neurology, Faculty of Medicine, Bandırma Onyedi Eylül University, Balıkesir, Türkiye, bandirma.edu.tr.<br /><searchLink fieldCode="AU" term="%22Aksu+Şahin+İ%22">Aksu Şahin İ</searchLink>; Department of Medical Genetics, Faculty of Medicine, Balıkesir University, Balıkesir, Türkiye, balikesir.edu.tr.<br /><searchLink fieldCode="AU" term="%22Üstebay+S%22">Üstebay S</searchLink>; Department of Pediatrics, Faculty of Medicine, Bandırma Onyedi Eylül University, Bandırma, Türkiye, bandirma.edu.tr.<br /><searchLink fieldCode="AU" term="%22Ünsel+Bolat+G%22">Ünsel Bolat G</searchLink>; Department of Child and Adolescent Psychiatry, Faculty of Medicine, Balıkesir University, Balıkesir, Türkiye, balikesir.edu.tr.<br /><searchLink fieldCode="AU" term="%22Bolat+H%22">Bolat H</searchLink>; Department of Medical Genetics, Faculty of Medicine, Balıkesir University, Balıkesir, Türkiye, balikesir.edu.tr.
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  Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2026 May 22; Vol. 2026, pp. 8058409. <i>Date of Electronic Publication: </i>2026 May 22 (<i>Print Publication: </i>2026).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>MEDLINE
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        Value: 10.1155/humu/8058409
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            NameFull: Aksu Şahin İ
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              Text: 2026 May 22
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