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Article

A novel missense mutation in the signal peptide of the human POMC gene: a possible additional link between early-onset type 2 diabetes and obesity

30 May 2012

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Share to Adipose Tissue and Metabolism
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22643178
DOI: 10.1038/ejhg.2012.103

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Related research

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A novel missense mutation in the signal peptide of the human POMC gene: a possible additional link between early-onset type 2 diabetes and obesityPMID 22643178Read ↗

60 YEARS OF POMC: The proopiomelanocortin gene: discovery, deletion and disease.Semantic proximity Read ↗

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A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.Semantic proximity Read ↗

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanismSemantic proximity Read ↗

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[POMC gene mutations in human].Semantic proximity Read ↗

Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome.Semantic proximity Read ↗

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