MeSH 搜索器

G(M2) Ganglioside

A glycosphingolipid that accumulates due to a deficiency of hexosaminidase A or B (BETA-N-ACETYLHEXOSAMINIDASES), or GM2 activator protein, resulting in GANGLIOSIDOSES, heredity metabolic disorders that include TAY-SACHS DISEASE and SANDHOFF DISEASE.
推出的年份: 1991(1975)
副标题
树号: D09.400.410.420.025.475.400, D10.390.470.025.475.400, D10.570.877.360.025.475.400
MeSH 单一 ID: D005678
进入的组:
  • Ganglioside GM2
  • GM2, Ganglioside
  • Tay-Sachs Disease Ganglioside
  • Ganglioside, Tay-Sachs Disease
  • Tay Sachs Disease Ganglioside
  • GM2 Ganglioside
  • Ganglioside, GM2
早前的内容:
  • Gangliosides (1974)

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