你即將離開本站

並前往https://iovs.arvojournals.org/article.aspx?articleid=2775607

In silico Characterization of Tyrp1 Molecular Docking and ...

Purpose : Oculocutaneous albinism type 3 (OCA3) is an autosomal recessive disorder caused by mutations in the TYRP1 gene. Tyrosinase-related protein 1 ...

確定！ 回上一頁

查詢 「TYRP1」的人也找了：

  1. TYRP1
    2.
  2. Tyrosinase
    3.
  3. tyrp1 gene albinism
    4.
  4. MC1R
    5.
  5. Tyrosinase gene
    6.
  6. MITF
    7.
  7. Papuan
    8.
  8. Tyrosinase structure
    9.