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  1. 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 disti...

    Authors: Jan-Bernd Funcke, Julia von Schnurbein, Belinda Lennerz, Georgia Lahr, Klaus-Michael Debatin, Pamela Fischer-Posovszky and Martin Wabitsch

    Citation: Molecular and Cellular Pediatrics 2014 1:3

    Content type: Review

    Published on:

  2. Fragile X is the most common form of inherited intellectual disability and the leading known genetic cause of autism. There is currently no cure or approved medication for fragile X although various drugs targ...

    Authors: Cara J Westmark

    Citation: Molecular and Cellular Pediatrics 2014 1:1

    Content type: Mini review

    Published on: