A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity - Concepedia

Concepedia

Publication | Open Access

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity

DOI Full Paper Access

73

Citations

41

References

2014

Year

Julien Philippe, Pieter Stijnen, David Meyre, Franck De Graeve, DorothĂŠe Thuillier, Jérôme Delplanque, Gàbor Gyapay, Olivier Sand, John W.M. Creemers, Philippe Froguel,

International Journal of Obesity

ObesityMetabolic SyndromeNonsense Loss-of-function MutationSignal TransductionSignaling PathwayMetabolic DisorderGeneticsGenetic EpidemiologyHuman ObesityMetabolic RegulationPcsk1 ContributesMedicineCell BiologyCell Signaling

References

	Year	Citations

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