你即將離開本站

並前往https://www.frontiersin.org/articles/10.3389/fped.2019.00245/full

A Novel Homozygous Frameshift Mutation in CCN6 Causing ...

Background: Progressive pseudorheumatoid dysplasia (PPRD) inherited in an autosomal recessive fashion, is a disabling disease, ...

確定！ 回上一頁

查詢 「Frameshift mutation」的人也找了：

  1. frameshift mutation中文
    2.
  2. Frameshift mutation
    3.
  3. 移碼突變
    4.
  4. Point mutation frameshift mutation
    5.
  5. Silent mutation
    6.
  6. Insertion mutation
    7.
  7. DNA mutation
    8.
  8. Nonsense mutation
    9.