Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene

Ítems similars

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  per: Higuchi, Shinji, et al.
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• Genetic analysis in Japanese patients with osteogenesis imperfecta: Genotype and phenotype spectra in 96 probands
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• Metaphyseal dysostosis type Schmid.
  per: Dimson, S. B.
  Publicat: (1968)