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

Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene.
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DOI:
10.1297/cpe.24.33
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发表时间:
2015-01
期刊:
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
影响因子:
--
通讯作者:
Tanaka H
Tanaka H
中科院分区:
其他
文献类型:
--
作者:
Hasegawa K;Higuchi Y;Yamashita M;Tanaka H

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