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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

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Description scientific article
Author/s

author: Alec Aeby  Kate E Chandler  Corinne De Laet  Daphna R Marom  Doriette M Soler  Uta Tacke  Julie S Prendiville  Evangeline Wassmer  Isabelle Desguerre  Hannah L Gornall  Pierre G Landrieu  Gabriella M A Forte  Marcin Szynkiewicz  Riyana Babul-Hirji  Gillian I. Rice  Ghada M Abdel-Salam  Christian G E L de Goede  Marlene Rio  Guy Helman  Davide Tonduti  Elisa Fazzi  Jean-Pierre Lin  Magnhild Rasmussen  Adeline Vanderver  Ronen Spiegel  Tiong Y Tan  Roberta Battini  BELEN PEREZ DUEÑAS  Geneviève Bernard  Agathe Roubertie  Lieven Lagae  Simona Orcesi  Flore Rozenberg  Ivana Olivieri  Kathryn J Swoboda  Koenraad Devriendt  David Chitayat  Enza Maria Valente  Marjo van der Knaap  Manuel Castro-Gago  Grace Vassallo  Roberta La Piana  Marie-Laure Moutard  Maha Zaki  Cristina Cereda  Diana Chase  Yanick J. Crow  William P Whitehouse  Cyril Goizet  Blanca Gener  Michael Fahey 

Publication date January 16, 2015
Language English
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