Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
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GSE223439 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [RNA-seq]
|
36 | Shiming Chen | Nov 08, 2023 | ||||
GSE223657 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [ChIP-seq]
|
16 | Shiming Chen | Nov 08, 2023 | ||||
GSE223658 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [Spec-seq]
|
16 | Shiming Chen | Nov 08, 2023 | ||||
GSE223659 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms
|
68 | Shiming Chen | Nov 08, 2023 |