Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | |
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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 |