Information for "Analysis regarding genotypephenotype connection inside Turkish sufferers together with inherited retinal condition simply by nextgen sequencing"
From EECH Central
Basic information
| Display title | Analysis regarding genotypephenotype connection inside Turkish sufferers together with inherited retinal condition simply by nextgen sequencing |
| Default sort key | Analysis regarding genotypephenotype connection inside Turkish sufferers together with inherited retinal condition simply by nextgen sequencing |
| Page length (in bytes) | 3,731 |
| Page ID | 1397189 |
| Page content language | English (en) |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 0 |
Page protection
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
Edit history
| Page creator | Crabplace22 (Talk | contribs) |
| Date of page creation | 10:28, 23 April 2024 |
| Latest editor | Crabplace22 (Talk | contribs) |
| Date of latest edit | 10:28, 23 April 2024 |
| Total number of edits | 1 |
| Total number of distinct authors | 1 |
| Recent number of edits (within past 90 days) | 1 |
| Recent number of distinct authors | 1 |
