Fibroblasts derived from patients with opsismodysplasia display SHIP2-specific cell migration and adhesion defects

Author:

Ghosh Somadri1,Huber Céline23,Siour Quentin23,Sousa Sérgio B.4,Wright Michael5,Cormier-Daire Valérie23,Erneux Christophe1ORCID

Affiliation:

1. IRIBHM; Campus Erasme; ULB Bâtiment C; Bruxelles Belgium

2. Department of Medical Genetics; Reference Center for Skeletal Dysplasia; INSERM UMR 1163; Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia; Paris Descartes-Sorbonne Paris Cité University; AP-HP; Institut Imagine; Paris France

3. Hôpital Universitaire Necker-Enfants Malades; Paris France

4. Medical Genetics Unit; Hospital Pediátrico; Centro Hospitalare Universitário de Coimbra; Coimbra Portugal

5. Northern Genetics Service; Newcastle-upon-Tyne Hospitals; Newcastle- upon-Tyne UK

Funder

The Fonds de la Recherche Scientifique Médicale

Télévie Fellowship (Belgium)

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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