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中文
在J:234422中，描述的是一种构建，它利用了特异性的神经元标记物Thy1.2的启动子，驱动了携带渐进性超大脑皮层萎缩相关突变p.A152T的完整人类MAPT（tau）基因的表达。
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
