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10.5152/eurasianjmed.2017.17039 http://scihub22266oqcxt.onion/10.5152/eurasianjmed.2017.17039 C5469843!5469843 !28638260     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\28638260 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Eurasian+J+Med 2017 ; 49 (2 ): 148-151 Nephropedia Template TP {{tp|p=28638260 |t=2017. Infantile Nephropathic Cystinosis: A Novel CTNS Mutation |pdf=|usr=}}{{28638260 }} gab.com Text Infantile Nephropathic Cystinosis: A Novel CTNS Mutation JO: Eurasian J Med http://www.kidney.de/pget.php?&tw=1&pmid=28638260 #FOAvip Cystinosis is a rare autosomal recessive metabolic disorder characterized by the accumulation of cystine in lysosomes, which results from defects in the carrier-mediated transport protein encoded by the CTNS gene. Infantile nephropathic cystinosis (INC) is one of the major complications of cystinosis. It is characterized by findings of Fanconi's syndrome within the first year of life. Here we report two patients with INC presenting with signs of Fanconi's syndrome and describe a novel CTNS mutation. Twit Text FOAVip Infantile Nephropathic Cystinosis: A Novel CTNS Mutation ????Eurasian J Med http://www.kidney.de/pget.php?&tw=1&pmid=28638260 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28638260 #FOAvip English Wikipedia <ref>{{Cite pmid|28638260 }}</ref> Infantile Nephropathic Cystinosis: A Novel CTNS Mutation #MMPMID28638260 Doneray H ; Aldahmesh M ; Yilmaz G ; Cinici E ; Orbak Z Eurasian J Med 2017[Jun]; 49 (2 ): 148-151 PMID28638260 show ga Cystinosis is a rare autosomal recessive metabolic disorder characterized by the accumulation of cystine in lysosomes, which results from defects in the carrier-mediated transport protein encoded by the CTNS gene. Infantile nephropathic cystinosis (INC) is one of the major complications of cystinosis. It is characterized by findings of Fanconi's syndrome within the first year of life. Here we report two patients with INC presenting with signs of Fanconi's syndrome and describe a novel CTNS mutation. äInfantile Nephropathic Cystinosis: A Novel CTNS Mutation (epmc).pdf DeepDyve Pubget Overpricing