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2. 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. Elbelt U; Trovato A; Kloth M; Gentz E; Finke R; Spranger J; Galas D; Weber S; Wolf C; König K; Arlt W; Büttner R; May P; Allolio B; Schneider JG J Clin Endocrinol Metab; 2015 Jan; 100(1):E119-28. PubMed ID: 25279498 [TBL] [Abstract][Full Text] [Related]
3. A novel germline ARMC5 mutation in a patient with bilateral macronodular adrenal hyperplasia: a case report. Liu Q; Tong D; Xu J; Yang X; Yi Y; Zhang D; Wang L; Zhang J; Zhang Y; Li Y; Chang L; Chen R; Guan Y; Yi X; Jiang J BMC Med Genet; 2018 Mar; 19(1):49. PubMed ID: 29587644 [TBL] [Abstract][Full Text] [Related]
4. Primary macronodular adrenal hyperplasia (PMAH) can be generated by a new ARMC5 germline variant (c.52C>T (p.Gln18X)). Zhang F; Lin X; Yu X Endocr J; 2020 Dec; 67(12):1179-1186. PubMed ID: 32713866 [TBL] [Abstract][Full Text] [Related]
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13. ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions. Mulatero P; Schiavi F; Williams TA; Monticone S; Barbon G; Opocher G; Fallo F J Hum Hypertens; 2016 Jun; 30(6):374-8. PubMed ID: 26446392 [TBL] [Abstract][Full Text] [Related]
14. ARMC5 mutations in a large French-Canadian family with cortisol-secreting β-adrenergic/vasopressin responsive bilateral macronodular adrenal hyperplasia. Bourdeau I; Oble S; Magne F; Lévesque I; Cáceres-Gorriti KY; Nolet S; Awadalla P; Tremblay J; Hamet P; Fragoso MC; Lacroix A Eur J Endocrinol; 2016 Jan; 174(1):85-96. PubMed ID: 26604299 [TBL] [Abstract][Full Text] [Related]
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20. A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasia. He WT; Wang X; Song W; Song XD; Lu YJ; Lv YK; He T; Yu XF; Hu SH BMC Med Genomics; 2021 May; 14(1):126. PubMed ID: 33971873 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]