Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family

Fibrodysplasia Ossificans Progressiva (FOP, MIM 135100) is a rare genetic disease that is often inherited sporadically in an autosomal dominant pattern. The disease manifests in early life with malformed great toes and, its episodic and progressive bone formation in skeletal muscle after trauma is l...

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Detalles Bibliográficos
Autores principales: Morovvati, Ziba, Morovvati, Saeid, Alishiri, Gholamhossein Alishiri, Moosavi, Seyed Hossein, Ranjbar, Reza, Bolouki Moghaddam, Yaser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933443/
https://www.ncbi.nlm.nih.gov/pubmed/24518978

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