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Zhuang et al: Identification of a rare variant of c.1777G>A (p.G593S) in the COL1A1 gene as the etiology of recurrent osteogenesis imperfecta by whole-exome sequencing https://t.co/B3vcpOouOV
Zhuang et al: Identification of a rare variant of c.1777G>A (p.G593S) in the COL1A1 gene as the etiology of recurrent osteogenesis imperfecta by whole-exome sequencing https://t.co/B3vcpOouOV