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Dive into the research topics of 'Association of mutations in SLC12A1 encoding the NKCC2 cotransporter with neonatal primary hyperparathyroidism'. Together they form a unique fingerprint.- Sort by
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Dong Li, Lifeng Tian, Cuiping Hou, Cecilia E. Kim, Hakon Hakonarson, Michael A. Levine
Research output: Contribution to journal › Article › peer-review