hexosaminidase

常見(jiàn)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)減少體內(nèi)的一種叫做己糖胺酶的供應(yīng)，而腦細(xì)胞用它來(lái)代謝過(guò)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-乙酰氨基己糖苷酶
• acetyl hexosaminidase
  乙酰氨基己糖苷酶
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