Intronic point mutation in the IL2RG gene causing X-linked severe combined immunodeficiency

Details 詳細情報について

• CRID

  1360574094199607552

• DOI

  10.1093/hmg/4.9.1693

• ISSN

  14602083

  09646906

• Web Site

  http://academic.oup.com/hmg/article-pdf/4/9/1693/1777482/4-9-1693.pdf

• Data Source

  • Crossref