论文信息 - Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia. - 字舞流文

Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia.

V. Plagnol | T. Vulliamy | I. Dokal | M. Velangi | A. Walne | M. Kirwan | U. Hossain | A. Ho