Work

[A Chinese girl with fibrodysplasia ossificans progressiva caused by a de novo mutation R206H in ACVR1 gene].

Year: 2008
Type: article
Study design: Case Report
Source: PubMed
Language: Chinese
Subfield: Rheumatology
Field: Medicine
Open Access status: closed
OpenAlex ID: W9067608
FWCI:
Cites: 32
Cited by: 5
Related to: 10