Information for "Whole exome sequencing within silico and also welldesigned research look at the connection with the GJB2 mutation sCys169Tyr along with deaf ness as well as advise a function to the TMEM59 gene within the hearing method"
From EECH Central
Basic information
| Display title | Whole exome sequencing within silico and also welldesigned research look at the connection with the GJB2 mutation sCys169Tyr along with deaf ness as well as advise a function to the TMEM59 gene within the hearing method |
| Default sort key | Whole exome sequencing within silico and also welldesigned research look at the connection with the GJB2 mutation sCys169Tyr along with deaf ness as well as advise a function to the TMEM59 gene within the hearing method |
| Page length (in bytes) | 3,651 |
| Page ID | 1395850 |
| Page content language | English (en) |
| Page content model | wikitext |
| Indexing by robots | Allowed |
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Edit history
| Page creator | Clubbronze93 (Talk | contribs) |
| Date of page creation | 08:24, 23 April 2024 |
| Latest editor | Clubbronze93 (Talk | contribs) |
| Date of latest edit | 08:24, 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 |
