| Accession | SAMC1560400 |
|---|---|
| Accession in Other Database | GSA-Human: HRS122713 |
| Sample name | F1F |
| Title | F1F |
| Sample type | Human sample |
| Organism | Homo sapiens |
| Description | Normal |
| Attributes | *This sample record contains additional controlled-access information that is avaiable from GSA-Human by requesting study HRA000485 in the GSA-Human system. |
| Release date | 2022-12-01 |
| BioProject Accession | PRJCA003969 |
| Submitter | LIN KEN (dir1865@163.com) |
| Organization | The Affiliated Hospital of Kunming Medical University |
| Submission date | 2023-06-18 |
| Resource name | Description |
|---|---|
| GSA-Human (1) | - |
| HRA000485 (Controlled Access) | Numerous independent researches of congenital sensorineural hearing loss (CSHL) or microtia have been performed. In contrast, the common molecular mechanism has not been reported, although some cases with both phenotypes of CSHL and microtia have been observed in previous researches.Our objective is to identify the common molecular mechanism of CSHL and microtia. |