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

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Main Authors: Endris, Volker (Author) , Hackmann, Karl (Author) , Neuhann, Teresa M. (Author) , Grasshoff, Ute (Author) , Bonin, Michael (Author) , Haug, Ulrich (Author) , Hahn, Gabriele (Author) , Schallner, Jens C. (Author) , Schröck, Evelin (Author) , Tinschert, Sigrid (Author) , Rappold, Gudrun (Author) , Moog, Ute (Author)
Format: Article (Journal) Editorial
Language:English
Published: 12 October 2010
In: American journal of medical genetics
Year: 2010, Volume: 152A, Issue: 11, Pages: 2908-2911
ISSN:1552-4833
DOI:10.1002/ajmg.a.33692
Online Access: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
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Author Notes: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
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Item Description:Gesehen am 16.03.2023
Physical Description:Online Resource
ISSN:1552-4833
DOI:10.1002/ajmg.a.33692

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