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中文
包含人类RBP3启动子、兔子β-珠蛋白内含子以及携带AACTT缺失导致渐进性视网膜光感受器退化的人类ELOVL4突变基因cDNA的质粒被构建了。M69-80品系经过6个转基因拷贝的整合，其在ONL区域显示出最高的表达水平。（来源：J:147112）
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 |
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References Literature
Title
PMID
Journal
Year
IF
