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中文
在第二外显子通过CRISPR/Cas9技术用两个sgRNAs和一个捐赠寡核苷酸创建了一个4个碱基的缺失(等位基因c.435_438delCCGG或c.439_442delCCGG)，这个缺失模式模拟了有先天性动脉导管未闭(PDA)家族中发现的一种情况。(来源：J:278067)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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
