Clinical Aspects and Current Therapeutic Approaches for FOP

Clinical Aspects and Current Therapeutic Approaches for FOP

Fibrodysplasia ossificans progressiva (FOP) is an extremely rare heritable disorder of connective tissues characterized by progressive heterotopic ossification in various skeletal sites. It is caused by gain-of-function mutations in the gene encoding activin A receptor type I (<i>ACVR1</i&g...

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Bibliographic Details
Main Author:	Hiroshi Kitoh
Format:	Article
Language:	English
Published:	MDPI AG 2020-09-01
Series:	Biomedicines
Subjects:	fibrodysplasia ossificans progressiva skeletal malformation heterotopic ossification clinical trials
Online Access:	https://www.mdpi.com/2227-9059/8/9/325

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