hexosaminidase
常見例句
- 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減少體內(nèi)的一種叫做己糖胺酶的供應(yīng),而腦細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-乙酰氨基己糖苷酶 - acetyl hexosaminidase
乙酰氨基己糖苷酶 返回 hexosaminidase