MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism
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Main Authors: | |
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Format: | Article |
Published: |
Springer-Verlag
2017
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Series: | VIRCHOWS ARCHIV
471 No. 3 |
doi: | 10.1007/s00428-017-2158-3 |
mtmt: | 3223945 |
Online Access: | http://publicatio.bibl.u-szeged.hu/13033 |
Physical Description: | 401-411 |
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ISSN: | 0945-6317 |