Monogenic forms of childhood obesity due to mutations in the leptin gene

DOI PDF PDF Web Site Web Site 1 Citations

Description

<jats:title>Abstract</jats:title> <jats:p>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.</jats:p>

Journal

Citations (1)*help

See more

Report a problem

Back to top