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

被引：0

作者：

Oueslati, S. ^{[2
]}

Mahjoub, R. ^{[2
]}

Hammami, S. ^{[3
]}

Amri, Y. ^{[1
]}

Fredj, S. Hadgj ^{[1
]}

Kammoun, I. ^{[4
]}

Messaoud, T. ^{[1
]}

Talbi, E. ^{[2
]}

机构：

[1] Bechir Hamza Childrens Hosp, Biochem & Mol Biol Lab, Res Lab LR00SP03, Tunis, Tunisia

[2] Natl Inst Nutr & Food Technol, Res Unit Mol Biol Appl Study Hyperlipoprot Diabet, Clin Biol Lab, Tunis, Tunisia

[3] Natl Inst Nutr & Food Technol, Clin Biol Lab, Tunis, Tunisia

[4] Natl Inst Nutr & Food Technol, Dept Endocrinol & Metab Dis, Tunis, Tunisia

来源：

CLINICA CHIMICA ACTA | 2024年 / 558卷

关键词：

D O I：

10.1016/j.cca.2024.118286

中图分类号：

R446 [实验室诊断]; R-33 [实验医学、医学实验];

学科分类号：

1001 ;

摘要：

P0737

引用

页数：2

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