Prenatal screening of the maternal drug-sensitive deafness gene A1555G
| Title | Prenatal screening of the maternal drug-sensitive deafness gene A1555G |
|---|---|
| Description | The mitochondrial A1555G mutation, is considered a hotspot for mutations associated with nonsyndromic (NSHL) and aminoglycoside-induced hearing loss (AIHL). The pathogenicity of the A1555G substitution has been confirmed in numerous pedigrees of various ethnic and geographic origins and in sporadic cases and additionally by in vitro studies. |
| Organism | Homo sapiens |
| Data Type | Clinical Research data |
| Data Accessibility | Controlled-access |
| BioProject | PRJCA028445 |
| Release Date | 2024-07-24 |
| Submitter | zhang meng (zhmeng7884@163.com) |
| Organization | Beijing Obstetrics and Gynecology Hospital, Capital Medical University |
| Submission Date | 2024-07-24 |
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| File ID | File Title | Number/Samples | File Type | File Size | File Suffix | Download Times | Download |
|---|---|---|---|---|---|---|---|
| OMIX006960-01 | 2. OMIX-SUBMIT-mtDNA 1555 | 69 | Clinical Research data | 9.5 KB | xlsx | 0 | Controlled |