MST1R mutation as a genetic cause of Lady Windermere syndrome

Eur Respir J. 2017 Jan 18;49(1):1601478. doi: 10.1183/13993003.01478-2016. Print 2017 Jan.

Katharina L Becker^{1

2}, Peer Arts^{3

2}, Martin Jaeger¹, Theodorus S Plantinga¹, Christian Gilissen³, Arjan van Laarhoven¹, Jakko van Ingen⁴, Joris A Veltman^{3

5}, Leo A B Joosten¹, Alexander Hoischen³, Mihai G Netea¹, Michael D Iseman⁶, Edward D Chan^{6

7

8}, Frank L van de Veerdonk⁹

¹ Dept of Internal Medicine, Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
² Both authors contributed equally.
³ Dept of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, The Netherlands.
⁴ Dept of Microbiology, Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
⁵ Dept of Clinical Genetics, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The Netherlands.
⁶ Dept of Medicine and Academic Affairs, National Jewish Health, Denver, CO, USA.
⁷ Dept of Medicine, Denver Veterans Affairs Medical Center, Denver, CO, USA.
⁸ Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical Campus, Denver, CO, USA.
⁹ Dept of Internal Medicine, Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands [email protected].

No abstract available

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