Biallelic loss of function variant in ZNF808 is associated with non-syndromic neonatal diabetes

被引：1
|
作者：
Alqahtani, Mohammad Awwad [1 ]
Al-Qahtani, Saleh M. M. [2 ]
Al-Falki, Yahya H. H. [3 ]
Alharby, Essa [4 ]
Albulym, Obaid Mohammed [5 ]
Almontashiri, Naif A. M. [4 ]
机构：
[1] Specialized Med Complex, Abha, Saudi Arabia
[2] King Khalid Univ, Coll Med, Dept Child Hlth, Abha, Saudi Arabia
[3] King Khalid Univ, Coll Med, Ophthalmol Dept, Abha, Saudi Arabia
[4] Taibah Univ, Ctr Genet & Inherited Dis, Al Madinah Al Munawwarah, Saudi Arabia
[5] King Khalid Univ, Fac Sci, Dept Biol, Abha, Saudi Arabia
来源：
CLINICAL GENETICS | 2023年 / 104卷 / 04期
关键词：
homozygous; loss-of-function; neonatal diabetes; recessive; ZNF808; GENOME-WIDE ASSOCIATION;
D O I：
10.1111/cge.14389
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：497 / 498
页数：2
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