CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations

Authors:	Verlaan Dominique J Laurent Sandra B Rochefort Daniel L Liquori Christina L Marchuk Douglas A Siegel Adrian M Rouleau Guy A

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