|
| Status |
Public on Feb 20, 2023 |
| Title |
Human germline biallelic complete NFAT1 deficiency causes the triad of joint contractures, osteochondromas, and susceptibility to B cell malignancy |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by high throughput sequencing
|
| Summary |
This SuperSeries is composed of the SubSeries listed below.
|
| |
|
| Overall design |
Refer to individual Series
|
| Web link |
https://pubmed.ncbi.nlm.nih.gov/35789258/
|
| |
|
| Citation(s) |
35789258 |
| Submission date |
Jan 10, 2022 |
| Last update date |
Feb 22, 2023 |
| Contact name |
Stuart E Turvey |
| E-mail(s) |
sturvey@cw.bc.ca
|
| Organization name |
BC Children's Hospital Research Institute
|
| Street address |
938 W 28th Ave
|
| City |
Vancouver |
| State/province |
BC |
| ZIP/Postal code |
V5Z 4H4 |
| Country |
Canada |
| |
|
| Platforms (2) |
| GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
| GPL30173 |
NextSeq 2000 (Homo sapiens) |
|
| Samples (20)
|
|
| This SuperSeries is composed of the following SubSeries: |
| GSE193410 |
Human germline biallelic complete NFAT1 deficiency causes the triad of joint contractures, osteochondromas, and susceptibility to B cell malignancy [Single] |
| GSE193414 |
Human germline biallelic complete NFAT1 deficiency causes the triad of joint contractures, osteochondromas, and susceptibility to B cell malignancy [Bulk] |
|
| Relations |
| BioProject |
PRJNA796049 |
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