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

Kosei Hasegawa, Yosuke Higuchi, Miho Yamashita, Hiroyuki Tanaka
  • Clinical Pediatric Endocrinology, January 2015, Japanese Society for Pediatric Endocrinology
  • DOI: 10.1297/cpe.24.33

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The following have contributed to this page: Dr Kosei Hasegawa and Dr Kosei Hasegawa