Results
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9321.
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Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. [electronic resource] by
- Vivero, M
- Cho, M T
- Begtrup, A
- Wentzensen, I M
- Walsh, L
- Payne, K
- Zarate, Y A
- Bosanko, K
- Schaefer, G B
- DeBrosse, S
- Pollack, L
- Mason, K
- Retterer, K
- DeWard, S
- Juusola, J
- Chung, W K
Producer: 20190415
In:
Clinical genetics vol. 91
Availability: No items available.
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