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Gene-modified neural progenitor cells for the treatment of neuropathic lysosomal storage diseases
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作者 oriana mandolfo Brian W.Bigger 《Neural Regeneration Research》 SCIE CAS CSCD 2023年第9期1954-1955,共2页
Lysosomal storage diseases:Lysosomal storage diseases(LSDs) are a family of about 70 disorders,with an overall incidence of 1:7000 live births.They are caused by dysfunctional lysosomal hydrolases,eventually leading t... Lysosomal storage diseases:Lysosomal storage diseases(LSDs) are a family of about 70 disorders,with an overall incidence of 1:7000 live births.They are caused by dysfunctional lysosomal hydrolases,eventually leading to the accumulation of undegraded substrate into the lysosome.This results in a wide array of symptoms,which may include:the presence of dysmorphic features,cardio-respiratory disease,bone and joint disease,organomegaly,developmental delay and neurocognitive decline.The majority of these diseases have a neurological component and in the absence of treatment. 展开更多
关键词 DISEASES PROGENITOR eventually
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