| Accession | PRJCA000774 |
|---|---|
| Title | PHA1 rare disease |
| Relevance | Medical |
| Data types | Exome |
| Organisms | Homo sapiens |
| Description | WES of familial PHA1 rare disease to find SNPs and Indels in PHA1 patients. Meanwhile, describe the genetic patten of the family. |
| Sample scope | Monoisolate |
| Release date | 2018-02-28 |
| Submitter | Zongzhi Liu (liuzongzhi@big.ac.cn) |
| Organization | Beijing Institute of Genomics, Chinese Academy of Sciences |
| Submission date | 2018-02-28 |
| Resource name | Description |
|---|---|
| BioSample (3) | - |
| SAMC025242 | PHA1 rare disease |
| SAMC025241 | PHA1 rare disease |
| SAMC025240 | PHA1 rare disease |
| GSA (1) | - |
| CRA000776 | PHA1 rare disease |