scholarly journals Novel mutations p.V220E and c.30G>T in menin gene are associated with hereditary predisposition to multiple endocrine neoplasia type 1

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Author(s):  
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Bartlomiej Budny ◽  
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Olena Leitgeber-Dominiczak ◽  
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2012 ◽  
Vol 76 (5) ◽  
pp. 719-724 ◽  
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