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

Research output: Contribution to journalComment/debate

2 Citations (Scopus)
Original languageEnglish
Pages (from-to)33-36
Number of pages4
Journalclinical pediatric endocrinology
Volume24
Issue number1
DOIs
Publication statusPublished - 2015
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

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