Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma (Q34810821)

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Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma
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    Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma (English)
    Alessia Trovato
    Michael Kloth
    Reinhard Finke
    David Galas
    Susanne Weber
    Cristina Wolf
    Katharina König
    Reinhard Büttner
    Jochen G Schneider
    1 January 2015

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