CLN3 transcript complexity revealed by long-read RNA sequencing analysis
Abstract Background Batten disease is a group of rare inherited neurodegenerative diseases. Juvenile CLN3 disease is the most prevalent type, and the most common pathogenic variant shared by most patients is the "1-kb" deletion which removes two internal coding exons (7 and 8) in CLN3. Pre...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2024-10-01T00:00:00Z.
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