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Mutations in AP2S1 cause familial hypocalciuric hypercalc... | ResearchHub
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Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3
0
Authors
M. Nesbit
15 more
M. Nesbit
•
Fadil Hannan
13 more
•
Rajesh Thakker
Published
December 9, 2012
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Journal
Nature Genetics
Topics
Biology
Physiology
Medicine
Internal Medicine
Cell Biology
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DOI
10.1038/ng.2492
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Supporters
Support the authors with ResearchCoin
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Journal
Nature Genetics
Topics
Biology
Physiology
Medicine
Internal Medicine
Cell Biology
Show all topics
DOI
10.1038/ng.2492
Other Formats
PDF
