Phenotypic differences of patients with fibrodysplasia ossificans progressive due to p.Arg258Ser variants of ACVR1.

Hum Genome Var · 2015 · PMC4785553 · PMID 27081558

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extremely significantno p-value reported

This report is extremely significant in terms of providing new evidence of symptoms experienced by patients with c.774G>T who present with clinical findings that are different from those of c.774G>C but in whom mutation occurs in the same amino acid.

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