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( 4 ), there has not been conclusive evidence for the discovery of highly penetrant NMTC genes. Recently, two studies implicated a germline missense variant (G534E) in the HABP2 gene as the cause of familial NMTC ( 5 , 6 ). Gara and coworkers ( 5
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. HABP2 p.G534E variant in patients with family history of thyroid and breast cancer . Oncotarget 2017 8 40896 – 40905 . ( https://doi.org/10.18632/oncotarget.16639 ) 54 Nieminen TT Walker CJ Olkinuora A Genutis LK O’Malley M Wakely PE