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

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...

Full description

Bibliographic Details
Main Authors: Ziba Morovvati, Saeid Morovvati, Gholamhossein Alishiri, Seyed Hossein Moosavi, Reza Ranjbar, Yaser Bolouki Moghaddam
Format: Article
Language:English
Published: Royan Institute (ACECR), Tehran 2014-03-01
Series:Cell Journal
Subjects:
FOP
c.617G>A Mutation
Online Access:http://www.celljournal.org/library/upload/article/af_362352274242483536245452777342428233575211-Morovati-1.pdf

Internet

http://www.celljournal.org/library/upload/article/af_362352274242483536245452777342428233575211-Morovati-1.pdf

Similar Items