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222.
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Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3. [electronic resource] by
- Nesbit, M Andrew
- Hannan, Fadil M
- Howles, Sarah A
- Reed, Anita A C
- Cranston, Treena
- Thakker, Clare E
- Gregory, Lorna
- Rimmer, Andrew J
- Rust, Nigel
- Graham, Una
- Morrison, Patrick J
- Hunter, Steven J
- Whyte, Michael P
- McVean, Gil
- Buck, David
- Thakker, Rajesh V
Producer: 20130222
In:
Nature genetics vol. 45
Availability: No items available.
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