Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1186/s40348-014-0003-1 http://scihub22266oqcxt.onion/10.1186/s40348-014-0003-1 C4644131!4644131!26567097     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Mol+Cell+Pediatr 2014 ; 1 (ä): ä Nephropedia Template TP {{tp|p=26567097|t=2014. Monogenic forms of childhood obesity due to mutations in the leptin gene |pdf=|usr=}}{{26567097}} gab.com Text Monogenic forms of childhood obesity due to mutations in the leptin gene JO: Mol Cell Pediatr http://www.kidney.de/pget.php?&tw=1&pmid=26567097 #FOAvip Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight distinct mutations found so far in humans. Twit Text FOAVip Monogenic forms of childhood obesity due to mutations in the leptin gene ????Mol Cell Pediatr http://www.kidney.de/pget.php?&tw=1&pmid=26567097 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26567097 #FOAvip English Wikipedia <ref>{{Cite pmid|26567097}}</ref> Monogenic forms of childhood obesity due to mutations in the leptin gene #MMPMID26567097 Funcke JB; von Schnurbein J; Lennerz B; Lahr G; Debatin KM; Fischer-Posovszky P; Wabitsch M Mol Cell Pediatr 2014[Dec]; 1 (ä): ä PMID26567097show ga Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight distinct mutations found so far in humans. äMonogenic forms of childhood obesity due to mutations in the leptin ge(epmc).pdf DeepDyve Pubget Overpricing