Insomnia, Fatal Familial
An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).
推出的年份: 2003
树号: C01.207.800.392, C10.228.228.800.392, C10.574.843.512, C10.886.425.800.800.400
MeSH 单一 ID: D034062
进入的组:
Fatal Familial Insomnias
Insomnias, Fatal Familial
Insomnia Familial Fatal
Familial Fatal, Insomnia
Familial Fatals, Insomnia
Fatal, Insomnia Familial
Fatals, Insomnia Familial
Insomnia Familial Fatals
Familial Fatal Insomnia
Familial Fatal Insomnias
Fatal Insomnia, Familial
Fatal Insomnias, Familial
Insomnia, Familial Fatal
Insomnias, Familial Fatal
Fatal Familial Insomnia
早前的内容:
Prion Diseases (1992-2002)
Sleep Initiation and Maintenance Disorders (1986-1992)
留言 (0)