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Article

The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressiva

9 Mar 2007

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17351709
DOI: 10.1007/s10038-007-0128-3

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The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressivaPMID 17351709Read ↗

ACVR1 gene mutation in sporadic Korean patients with fibrodysplasia ossificans progressiva.Semantic proximity Read ↗

Fibrodysplasia Ossificans Progressiva: Clinical Course, Genetic Mutations and Genotype-Phenotype CorrelationSemantic proximity Read ↗

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A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patients.Semantic proximity Read ↗

A unique case of fibrodysplasia ossificans progressiva with an <i>ACVR1</i> mutation, G356D, other than the common mutation (R206H)Semantic proximity Read ↗

Fibrodysplasia Ossificans Progressiva: What Have We Achieved and Where Are We Now? Follow-up to the 2015 Lorentz Workshop.Semantic proximity Read ↗

Mutational screening of <i>ACVR1</i> gene in Brazilian fibrodysplasia ossificans progressiva patientsSemantic proximity Read ↗

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.Semantic proximity Read ↗

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Challenges in the diagnosis of fibrodysplasia ossificans progressiva with the ACVR1 mutation (c.774G > C, p.R258S): a case report and review of literature.Semantic proximity Read ↗

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