Identification and Molecular Analysis of a Potential Disease-causing Mutation in gene A in Congenital Radioulnar Synostosis
Identification and Molecular Analysis of a Potential Disease-causing Mutation in gene A in Congenital Radioulnar Synostosis
批准号:
16K10852
负责人:
Kato Hiroyuki
金额:
$3.0万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2016
资助国家:
日本
项目状态:
已结题
起止时间:
2016-04-01 至 2019-03-31
中文摘要
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英文摘要
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
先天性橈尺骨癒合症における原因遺伝子検索
寻找先天性桡尺骨骨联结的致病基因
DOI:
--
发表时间:
2017
期刊:
影响因子:
--
作者:
[小松雅俊、河村太介,中村幸男,鈴木孝子, 喜久川真悟,松原光宏,岩川紘子, 内山茂晴,林正徳, 岩崎倫政,加藤博之]
通讯作者:
岩崎倫政,加藤博之
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依托单位: