hexosaminidase
常见例句
- 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.
由基因突变导致的山德霍夫氏病会减少体内的一种叫做己糖胺酶的供应,而脑细胞用它来代谢过多的脂质。 - 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