Effects of Alexander Disease Causing Mutations on Glial Fibrillary Acidic Protein Filament Assembly and Stability
碩士 === 國立清華大學 === 分子醫學研究所 === 103 === Alexander disease (AxD) is a primary genetic disorder of astrocytes caused by heterozygous mutations in GFAP, which encodes the major astrocyte intermediate filament protein, glial fibrillary acidic protein (GFAP). The mechanism of GFAP mutation causing the AxD...
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| Format: | Others |
| Language: | en_US |
| Published: |
2015
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| Online Access: | http://ndltd.ncl.edu.tw/handle/02405757195378264955 |