Concepedia

Molecular and Clinical Evidence for an<i>ARMC5</i>Tumor Syndrome: Concurrent Inactivating Germline and Somatic Mutations Are Associated With Both Primary Macronodular Adrenal Hyperplasia and Meningioma

Ulf Elbelt, Alessia Trovato, Michael Kloth, Enno Gentz, R. Finke, Joachim Spranger, David J. Galas, Susanne N. Weber, Cristina Wolf, Katharina König,

The Journal of Clinical Endocrinology & Metabolism · 2014 · 104 citations · 47 references

Open access

Abstract

Our analysis further confirms inherited inactivating ARMC5 mutations as a cause of familial PMAH and suggests an additional role for the development of concomitant intracranial meningiomas.

References

47

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