Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies

Author:

Arts Peer,Simons Annet,AlZahrani Mofareh S.,Yilmaz Elanur,AlIdrissi Eman,van Aerde Koen J.,Alenezi Njood,AlGhamdi Hamza A.,AlJubab Hadeel A.,Al-Hussaini Abdulrahman A.,AlManjomi Fahad,Alsaad Alaa B.,Alsaleem Badr,Andijani Abdulrahman A.,Asery Ali,Ballourah Walid,Bleeker-Rovers Chantal P.,van Deuren Marcel,van der Flier Michiel,Gerkes Erica H.,Gilissen Christian,Habazi Murad K.,Hehir-Kwa Jayne Y.,Henriet Stefanie S.,Hoppenreijs Esther P.,Hortillosa Sarah,Kerkhofs Chantal H.,Keski-Filppula Riikka,Lelieveld Stefan H.,Lone Khurram,MacKenzie Marius A.,Mensenkamp Arjen R.,Moilanen Jukka,Nelen Marcel,ten Oever Jaap,Potjewijd Judith,van Paassen Pieter,Schuurs-Hoeijmakers Janneke H. M.,Simon Anna,Stokowy Tomasz,van de Vorst Maartje,Vreeburg Maaike,Wagner Anja,van Well Gijs T. J.,Zafeiropoulou Dimitra,Zonneveld-Huijssoon Evelien,Veltman Joris A.,van Zelst-Stams Wendy A. G.,Faqeih Eissa A.,van de Veerdonk Frank L.,Netea Mihai G.,Hoischen Alexander

Funder

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

European Research Council

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine

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