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Comparison of Leptin Protein Levels in Prader-Willi Syndrome and Control Individuals

Prader-Willi syndrome (PWS) is characterized by early childhood obesity, mental deficiency, hypogonadism, hypotonia, hypopigmentation, short stature, small hands and feet, and a characteristic face. It is the most common genetic cause of obesity and obesity is the most significant health problem for...

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Detalhes bibliográficos
Publicado no:Am J Med Genet
Main Authors: Butler, Merlin G., Moore, Jason, Morawiecki, Andrew, Nicolson, Margery
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6775636/
https://ncbi.nlm.nih.gov/pubmed/9450849
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