Joint-specific risk of impaired function in fibrodysplasia ossificans progressiva (FOP)

Author:

Pignolo Robert J.,Durbin-Johnson Blythe P.,Rocke David M.,Kaplan Frederick S.

Funder

International Fibrodysplasia Ossificans Progressiva Association (IFOPA)

Center for Research in FOP and Related Disorders

Ian Cali Endowment for FOP Research

Whitney Weldon Endowment for FOP Research

Isaac and Rose Nassau Professorship of Orthopaedic Molecular Medicine

Ian Cali Distinguished Clinician-Scientist

Robert and Arlene Kogod Professorship in Geriatric Medicine

Radiant Hope Foundation

National Center for Advancing Translational Sciences

National Institutes of Health

University of California Davis School of Medicine

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference18 articles.

1. Clinical utility gene card for: Fibrodysplasia ossificans progressiva;Bravenboer;Eur. J. Hum. Genet.,2015

2. Fibrodysplasia ossificans progressiva;Kaplan;Best Pract. Res. Clin. Rheumatol.,2008

3. Fibrodysplasia ossificans progressiva: clinical and genetic aspects;Pignolo;Orphanet J. Rare Dis.,2011

4. Fibrodysplasia ossificans progressiva: diagnosis, management, and therapeutic horizons;Pignolo;Pediatr. Endocrinol. Rev.,2013

5. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat. Genet.,2006

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