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

doi:10.1297/cpe.24.33

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

University Hospital

Research output: Contribution to journal › Comment/debate › peer-review

3 Citations (Scopus)

Original language	English
Pages (from-to)	33-36
Number of pages	4
Journal	clinical pediatric endocrinology
Volume	24
Issue number	1
DOIs	https://doi.org/10.1297/cpe.24.33
Publication status	Published - 2015

ASJC Scopus subject areas

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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1297/cpe.24.33

Cite this

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

author = "Kosei Hasegawa and Yosuke Higuchi and Miho Yamashita and Hiroyuki Tanaka",

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AU - Higuchi, Yosuke

AU - Yamashita, Miho

AU - Tanaka, Hiroyuki

PY - 2015

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M3 - Comment/debate

AN - SCOPUS:84922439077

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JO - clinical pediatric endocrinology

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

ASJC Scopus subject areas

UN SDGs

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