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14:00–14:15
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W7-001 |
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia (COMA)
Gökhan Yigit (Göttingen/DE) Redezeit: 15 min |
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14:15–14:30
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W7-002 |
Towards a targeted drug therapy for Best vitelliform macular dystrophy
Andrea Milenkovic (Regensburg/DE) Redezeit: 15 min |
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14:30–14:45
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W7-003 |
RB1-negative organoids model retinoblastoma with proliferation of cone photoreceptors and loss of retinal cell type differentiation
Deniz Kanber (Essen/DE) Redezeit: 15 min |
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14:45–15:00
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W7-004 |
Decipher transcription regulation of the human SNCA gene via THAP1 revealed a critical role of its enhancers
Fubo Cheng (Tuebingen/DE) Redezeit: 15 min |
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15:00–15:15
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W7-005 |
Muscle weakness in patients suffering from AAMR syndrome is caused by α-Dystroglycan hyperglycosylation
Patricia Franzka (Jena/DE) Redezeit: 15 min |
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15:15–15:30
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W7-006 |
The novel stress-responsive gene Gdpgp1/mcp-1 in neuronal cells
Alexander Schulz (Jena/DE) Redezeit: 15 min |
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