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McCooke et al., 2012 - Google Patents

A novel mutation causing nephronophthisis in the Lewis polycystic kidney rat localises to a conserved RCC1 domain in Nek8

McCooke et al., 2012

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Document ID
16623170122176559394
Author
McCooke J
Appels R
Barrero R
Ding A
Ozimek-Kulik J
Bellgard M
Morahan G
Phillips J
Publication year
Publication venue
BMC genomics

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Background Nephronophthisis (NPHP) as a cause of cystic kidney disease is the most common genetic cause of progressive renal failure in children and young adults. NPHP is characterized by abnormal and/or loss of function of proteins associated with primary cilia …
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