MeSH 搜索器

Bulbo-Spinal Atrophy, X-Linked

An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
推出的年份: 2009(2000)
副标题
树号: C10.228.854.468.399, C10.574.500.175, C10.574.562.500.374, C10.668.467.500.186, C16.320.322.076, C16.320.400.100
MeSH 单一 ID: D055534
进入的组:
  • Bulbo Spinal Atrophy, X Linked
  • Bulbospinal Muscular Atrophy, X-linked
  • Bulbospinal Muscular Atrophy, X linked
  • Kennedy Spinal and Bulbar Muscular Atrophy
  • Spinal and Bulbar Muscular Atrophy
  • X-linked Bulbospinal Muscular Atrophy
  • X linked Bulbospinal Muscular Atrophy
  • Kennedy's Disease
  • Spinobulbar Muscular Atrophy
  • Spinal And Bulbar Muscular Atrophy, X-Linked 1
  • Spinal And Bulbar Muscular Atrophy, X Linked 1
  • Kennedy Syndrome
  • X-Linked Bulbo-Spinal Atrophy
  • Atrophies, X-Linked Bulbo-Spinal
  • Atrophy, X-Linked Bulbo-Spinal
  • Bulbo-Spinal Atrophies, X-Linked
  • X Linked Bulbo Spinal Atrophy
  • X-Linked Bulbo-Spinal Atrophies
  • Atrophy, Muscular, Spinobulbar
  • Muscular Atrophy, Spinobulbar
  • Atrophy, Spinobulbar Muscular
  • Spinobulbar Muscular Atrophies
  • Kennedy Disease
  • X-Linked Spinal and Bulbar Muscular Atrophy
  • X Linked Spinal and Bulbar Muscular Atrophy

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