Information for "The 1st document regarding 2 homozygous sequence variants throughout FKRP as well as SELENON genetics linked to syndromic congenital buff dystrophy throughout Iran Additional growth of the actual medical phenotypes"
From EECH Central
Basic information
| Display title | The 1st document regarding 2 homozygous sequence variants throughout FKRP as well as SELENON genetics linked to syndromic congenital buff dystrophy throughout Iran Additional growth of the actual medical phenotypes |
| Default sort key | The 1st document regarding 2 homozygous sequence variants throughout FKRP as well as SELENON genetics linked to syndromic congenital buff dystrophy throughout Iran Additional growth of the actual medical phenotypes |
| Page length (in bytes) | 3,429 |
| Page ID | 1434429 |
| 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 | Locketpea5 (Talk | contribs) |
| Date of page creation | 11:40, 3 May 2024 |
| Latest editor | Locketpea5 (Talk | contribs) |
| Date of latest edit | 11:40, 3 May 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 |
