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Correspondence on "Phenylalanine hydroxylase deficiency diagnosis and management: a 2023 evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)" by Smith et al

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Main Authors: Burgard, Peter (Author) , Ballhausen, Diana (Author) , Hennermann, Julia B. (Author) , Hoffmann, Georg F. (Author) , Kölker, Stefan (Author) , Konstantopoulou, Vassiliki (Author) , Lachmann, Robin (Author) , Maier, Esther M. (Author) , Murphy, Elaine (Author) , Ullrich, Kurt (Author) , Ziagaki, Athanasia (Author) , Zschocke, Johannes (Author) , Lindner, Martin (Author)
Format: Article (Journal) Editorial
Language:English
Published: January 2026
In: Genetics in medicine
Year: 2026, Volume: 28, Issue: 1, Pages: 1-3
ISSN:1530-0366
DOI:10.1016/j.gim.2025.101600
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.gim.2025.101600
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S1098360025002473
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Author Notes:Peter Burgard, Diana Ballhausen, Julia B. Hennermann, Georg F. Hoffmann, Stefan Kölker, Vassiliki Konstantopoulou, Robin Lachmann, Esther M. Maier, Elaine Murphy, Kurt Ullrich, Athanasia Ziagaki, Johannes Zschocke, Martin Lindner
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Item Description:Gesehen am 25.03.2026
Physical Description:Online Resource
ISSN:1530-0366
DOI:10.1016/j.gim.2025.101600

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