Nephronophthisis

NPHP is the most common monogenic cause of CKD in children or adolescents. Extra-renal symptoms often accompany, therefore examination of retina, hearing, and skeleton is necessary in patients with CKD with insidious onset. Genes involved in NPHP-RC are mostly related in primary cilia. While genetic...

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Main Authors: Hee Gyung Kang (Author), Hae Il Cheong (Author)
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出版: Korean Society of Pediatric Nephrology, 2015-04-01T00:00:00Z.
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3rd Floor Main Library

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索引号: A1234.567
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