hexosaminidase

基本解釋

• n.[生化]己糖胺酶；氨基己糖苷酶

同根派生

• hexosaminidase相關(guān)詞

英漢例句

• Sandhoff results from a genetic mutation that reduces the body's supply of an enzyme, called hexosaminidase ("hex"), used by brain cells to metabolize excess fatty material called lipids.
  由基因突變導(dǎo)致的山德霍夫氏病會(huì)減少躰內(nèi)的一種叫做己糖胺酶的供應(yīng)，而腦細(xì)胞用它來代謝過多的脂質(zhì)。
• Hexosaminidase A and B deficiency
  己糖胺酶A和B缺乏
• Hexosaminidase activator deficiency
  己糖胺酶激活因子缺乏
• Severe hexosaminidase A deficiency
  重度己糖胺酶A缺乏
• N-acetyl hexosaminidase
  N-乙醯氨基己糖苷酶

• hexosaminidase更多例句