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Volumn 120, Issue 3, 2010, Pages 791-802

Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076);Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

(55)  O'Toole, John F a   Liu, Yangjian b   Davis, Erica E b,c   Westlake, Christopher J d   Attanasio, Massimo a   Otto, Edgar A a   Seelow, Dominik e,f   Nurnberg, Gudrun e   Becker, Christian e   Nuutinen, Matti g   Kärppä, Mikko g   Ignatius, Jaakko g   Uusimaa, Johanna g   Pakanen, Salla g   Jaakkola, Elisa g   Van Den Heuvel, Lambertus P h   Fehrenbach, Henry i   Wiggins, Roger j   Goyal, Meera j   Zhou, Weibin a   more..


Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL PROTEIN; PROLINE; UNCLASSIFIED DRUG; X PROLYL AMINOPEPTIDASE 3;

EID: 77949865316     PISSN: 00219738     EISSN: 15588238     Source Type: Journal    
DOI: 10.1172/JCI40076C1     Document Type: Erratum
Times cited : (99)

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