MeSH 搜索器

Hexosaminidase B

A mammalian beta-hexosaminidase isoform that is comprized of hexosaminidase beta subunits. Deficiency of hexosaminidase B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.
推出的年份: 2008
副标题
树号: D08.811.277.450.483.180.875
MeSH 单一 ID: D054819
进入的组:
  • Hex B
早前的内容:
  • beta-N-Acetylhexosaminidases (1987-2007)

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