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RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference. [electronic resource] by
- Etzler, J
- Peyrl, A
- Zatkova, A
- Schildhaus, H-U
- Ficek, A
- Merkelbach-Bruse, S
- Kratz, C P
- Attarbaschi, A
- Hainfellner, J A
- Yao, S
- Messiaen, L
- Slavc, I
- Wimmer, K
Producer: 20080207
In:
Human mutation vol. 29
Availability: No items available.
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