SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome

被引：0
|
作者：
Hacihamdioglu, Duygu Ovunc [1 ]
Altan Ferhatoglu, Zeynep [2 ]
Karkucak, Mutlu [3 ]
Fisek Izci, Neslihan Muge [2 ]
Yakut, Tahsin [3 ]
机构：
[1] Bahcesehir Univ, Med Pk Goztepe Hosp, Div Pediat Nephrol, Med Fac,Dept Pediat, Istanbul, Turkey
[2] Bahcesehir Univ, Med Pk Goztepe Hosp, Med Fac, Dept Dermatol, Istanbul, Turkey
[3] Istinye Univ, Genet Dis Assessment Ctr, Istanbul, Turkey
来源：
PEDIATRICS INTERNATIONAL | 2022年 / 64卷 / 01期
关键词：
filaggrin; Netherton syndrome; SPINK5; MANIFESTATIONS;
D O I：
10.1111/ped.15087
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页数：3
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