Phenotypic and molecular insights into CASK-related disorders in males

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Bibliographische Detailangaben
Hauptverfasser: Moog, Ute (VerfasserIn) , Bierhals, Tatjana (VerfasserIn) , Brand, Kristina (VerfasserIn)
Weitere Verfasser: Bautsch, Jan (BerichterstatterIn) , Biskup, Saskia (BerichterstatterIn) , Brune, Thomas (BerichterstatterIn) , Denecke, Jonas (BerichterstatterIn) , Die-Smulders, Christine E. de (BerichterstatterIn) , Evers, Christina (BerichterstatterIn) , Hempel, Maja (BerichterstatterIn) , Henneke, Marco (BerichterstatterIn) , Yntema, Helger (BerichterstatterIn) , Menten, Björn (BerichterstatterIn) , Pietz, Joachim (BerichterstatterIn) , Pfundt, Rolph (BerichterstatterIn) , Schmidtke, Jörg (BerichterstatterIn) , Steinemann, Doris (BerichterstatterIn) , Stumpel, Constance T. (BerichterstatterIn) , Maldergem, Lionel Van (BerichterstatterIn) , Kutsche, Kerstin (BerichterstatterIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2015
In: Orphanet journal of rare diseases
Year: 2015, Jahrgang: 10
ISSN:1750-1172
Online-Zugang:Verlag, Abstract, Volltext: http://www.ojrd.com/content/10/1/44/abstract
Volltext

MARC

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