Identification of a new mutation in the MEN1 gene responsible for familial primary hyperparathyroidism in a Tunisian family

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Bibliographic Details
Published in:Clinica chimica acta 2024-05, Vol.558, p.118286, Article 118286
Main Authors: Oueslati, S., Mahjoub, R., Hammami, S., Amri, Y., Hadgj Fredj, S., Kammoun, I., Messaoud, T., Talbi, E.
Format: Article
Language:English
Online Access:Get full text
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ISSN:0009-8981
1873-3492
DOI:10.1016/j.cca.2024.118286