Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia

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Hauptverfasser: Endris, Volker (VerfasserIn) , Hackmann, Karl (VerfasserIn) , Neuhann, Teresa M. (VerfasserIn) , Grasshoff, Ute (VerfasserIn) , Bonin, Michael (VerfasserIn) , Haug, Ulrich (VerfasserIn) , Hahn, Gabriele (VerfasserIn) , Schallner, Jens C. (VerfasserIn) , Schröck, Evelin (VerfasserIn) , Tinschert, Sigrid (VerfasserIn) , Rappold, Gudrun (VerfasserIn) , Moog, Ute (VerfasserIn)
Dokumenttyp: Article (Journal) Editorial
Sprache:Englisch
Veröffentlicht: 12 October 2010
In: American journal of medical genetics
Year: 2010, Jahrgang: 152A, Heft: 11, Pages: 2908-2911
ISSN:1552-4833
DOI:10.1002/ajmg.a.33692
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ajmg.a.33692
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.a.33692
Volltext
Verfasserangaben:Volker Endris, Karl Hackmann, Teresa M. Neuhann, Ute Grasshoff, Michael Bonin, Ulrich Haug, Gabriele Hahn, Jens C. Schallner, Evelin Schröck, Sigrid Tinschert, Gudrun Rappold, and Ute Moog

MARC

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