Showing results 1 to 2 of 2
| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Determination of DLC1 isoform 1 (DLC1-i1) as a gene therapy for the treatment of spinal muscular atrophy Proceeding/Conference:Selected Late Breaking News Oral Presentation. World Muscle Society Congress 2022 | 2022 | |||
A powerful questionnaire-based screening tool for congenital prosopangnosia Proceeding/Conference:International Congress of Psychology | 2008 | 82 |