Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
Karin R. Engelhardt(The Royal Free Hospital), Sean McGhee(University of California, Los Angeles), Sabine Winkler(The Royal Free Hospital), Atfa Sassi(Institut Pasteur de Tunis), Cristina Woellner(The Royal Free Hospital), Gabriela López‐Herrera(The Royal Free Hospital), Andrew Chen(University of California, Los Angeles), Hong Sook Kim(University of California, Los Angeles), Maria Garcia Lloret(University of California, Los Angeles), Ilka Schulze(University Medical Center Freiburg), Stephan Ehl(University Medical Center Freiburg), Jens Thiel(University Medical Center Freiburg), Dietmar Pfeifer(University Medical Center Freiburg), Hendrik Veelken(University Medical Center Freiburg), Tim Niehues(Helios Klinikum Krefeld), Kathrin Siepermann(Helios Klinikum Krefeld), Sebastian Weinspach(Heinrich Heine University Düsseldorf), İsmail Reisli(Selçuk University), Sevgi Keleş(Selçuk University), Ferah Genel(Dr. Behçet Uz Çocuk Hastalıkları Hastanesi), Necil Kutuculer(Ege University), Yıldız Çamcıoğlu(Istanbul University), Ayper Somer(Istanbul University), Elif Karakoç-Aydıner(Marmara University), Işıl Barlan(Marmara University), Andrew R. Gennery(Newcastle University), Ayşe Metìn, Aydan Değerli̇yurt, Maria Cristina Pietrogrande(University of Milan), Mehdi Yeganeh(Children's Medical Center), Zeina Baz(Saint George Hospital), Salem Al‐Tamemi(Sultan Qaboos University), Christoph Klein(Medizinische Hochschule Hannover), Jennifer M. Puck(University of California, San Francisco), Steven M. Holland(National Institutes of Health), Edward R.B. McCabe(Center for Human Genetics), Bodo Grimbacher(The Royal Free Hospital), Talal A. Chatila(University of California, Los Angeles)
Cited by 524Open Access
Abstract
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