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pro vyhledávání: '"張志萱"'
Autor:
Chang, Chih Hsuan, 張志萱
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 muta
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 muta
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/02405757195378264955
