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ataxia of charlevoix-saguenay
释义
ataxia of Charlevoix-Saguenay
ataxia of Charlevoix-Saguenay
an autosomal recessive, slowly progressive spastic ataxia of childhood onset, due to a gene mutation on chromosome 13.
[Saguenay-Lac-St. Jean and Charlevoix, isolated regions in northeastern Quebec to which the gene pool of the disease is limited]
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rhopalocera
rhopaloceral
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rhopalodinidae
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rhoptries
rhoptry
rhoptry-associated protein 1
rho/rac gef
rho/rac guanine nucleotide exchange factor fgd1
rhorc
rhos
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rhosp
rhost
rhos y-brithdir
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更新时间:2024/12/23 0:24:51