PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis

Author:

Arts Florence A.1,Sciot Raf2,Brichard Bénédicte3,Renard Marleen4,de Rocca Serra Audrey1,Dachy Guillaume1,Noël Laura A.1,Velghe Amélie I.1,Galant Christine5,Debiec-Rychter Maria6,Van Damme An3,Vikkula Miikka78,Helaers Raphaël7,Limaye Nisha7,Poirel Hélène A.79,Demoulin Jean-Baptiste1

Affiliation:

1. de Duve Institute, Université Catholique de Louvain, Brussels BE-1200, Belgium

2. Department of Pathology, University Hospitals Leuven and KU Leuven, Leuven BE-3000, Belgium

3. Department of Pediatric Hematology and Oncology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels BE-1200, Belgium

4. Department of Pediatric Hemato-oncology, University Hospitals Leuven, Leuven BE-3000, Belgium

5. Department of Pathology, Cliniques Universitaires Saint-Luc, Brussels BE-1200, Belgium

6. Department of Human Genetics, KU Leuven and University Hospitals, Leuven BE-3000, Belgium

7. Human Molecular Genetics, de Duve Institute, Université Catholique de Louvain, Brussels BE-1200, Belgium

8. Walloon Excellence in Life sciences and Biotechnology (WELBIO)

9. Center for Human Genetics, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels BE-1200, Belgium

Funder

Fonds National de la Recherche Scientifique, FNRS

FRFS-WELBIO

Publisher

Oxford University Press (OUP)

Subject

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

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