TagTeam :: Type XV osteogenesis imperfecta: A novel mutation in the <em>WNT1</em> gene, c.620G >A (p.R207H), is associated with an inner ear deformity - pubmed: wnt1 - Exome

Home Exome pubmed: wnt1 Type XV osteogenesis imperfecta: A novel mutation in the <em>WNT1</em> gene, c.620G >A (p.R207H), is associated with an inner ear deformity