search

MeSH 搜索器

Mannosidase Deficiency Diseases

Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
推出的年份: 2004
副标题
树号: C16.320.565.202.607, C16.320.565.595.577, C18.452.648.202.607, C18.452.648.595.577
MeSH 单一 ID: D044904
进入的组:
  • Deficiency Disease, Mannosidase
  • Deficiency Diseases, Mannosidase
  • Diseases, Mannosidase Deficiency
  • Mannosidase Deficiency Disease
  • Mannosidase Deficiency Syndromes
  • Deficiency Syndrome, Mannosidase
  • Deficiency Syndromes, Mannosidase
  • Mannosidase Deficiency Syndrome
  • Mannosidosis
  • Mannosidoses
早前的内容:
  • Mannosidosis (1984-2003)

留言 (0)

沒有登入
gif