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
收藏
页数：2
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