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Paper Details

Shared ACVR1 mutations in FOP and DIPG: Opportunities and challenges in extending biological and clinical implications across rare diseases.
Bone
18
2018
), ACVR1, ACVR1 mutations, DIPG, DIPGs, Diffuse Intrinsic Pontine Gliomas, FOP, Fibrodysplasia Ossificans Progressiva, Type I Bone Morphogenic Protein (BMP) receptor, autosomal dominant disorder, brain tumor, pediatric, rare diseases, tumor
Author NameAffiliation
Harry J HanThe Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania
Payal JainThe Children's Hospital of Philadelphia, United States Center for Data Driven Discovery in Biomedicine, Perelman School of Medicine at the University of Pennsylvania
Payal JainThe Children's Hospital of Philadelphia, United States Center for Data Driven Discovery in Biomedicine, Perelman School of Medicine at the University of Pennsylvania
Adam C ResnickThe Children's Hospital of Philadelphia, United States Center for Data Driven Discovery in Biomedicine, United States Center for Childhood Cancer Research, Perelman School of Medicine at the University of Pennsylvania
Adam C ResnickThe Children's Hospital of Philadelphia, United States Center for Data Driven Discovery in Biomedicine, United States Center for Childhood Cancer Research, Perelman School of Medicine at the University of Pennsylvania
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Release 1.2