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Proteasome impairment in neural cells derived from HMSN-P patient iPSCs
Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a heterozygous mutation (P285L) in Tropomyosin-receptor kinase Fused Gene (TFG), histopathologically characterized by progressive spinal motor neuron loss with TFG cytosolic aggregates. Although the TFG...
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Publicado no: | Mol Brain |
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Main Authors: | , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2017
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5310050/ https://ncbi.nlm.nih.gov/pubmed/28196470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-017-0286-y |
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