A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH)_2 vitamin D levels
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概要
- 論文の詳細を見る
- 2011-08-01
著者
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Sharma Amita
Pediatric Nephrology Unit Massachusetts General Hospital For Children And Harvard Medical School
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LINSHAW Micheal
Pediatric Nephrology Unit, Massachusetts General Hospital for Children and Harvard Medical School
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Linshaw Micheal
Pediatric Nephrology Unit Massachusetts General Hospital For Children And Harvard Medical School