题名 | A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family |
链接 | http://www.ncbi.nlm.nih.gov/pubmed/?term=A+novel+frameshift+mutation+in+FGA+(c.1846+del+A)+leading+to+congenital+a%EF%AC%81brinoge-+nemia+in+a+consanguineous+Syrian+family. |
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