Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na plus /Glucose Cotransporter Gene

被引:5
作者
Atay, Funda Yavanoglu [1 ]
Derme, Turan [1 ]
Uras, Nurdan [1 ]
Ceylaner, Gulay [2 ]
Ceylaner, Serdar [2 ]
Sari, Fatma Nur [1 ]
Oguz, Serife Suna [1 ]
机构
[1] Zekai Tahir Burak Matern Teaching Hosp, Neonatal Intens Care Unit, TR-06230 Ankara, Turkey
[2] Intergen Genet Res Ctr, Ankara, Turkey
关键词
Glucose-galactose malabsorption; SLC5A1; Neonatal diarrhea;
D O I
10.1007/s10620-016-4348-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
[No abstract available]
引用
收藏
页码:280 / 281
页数:2
相关论文
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[1]   GLUCOSE GALACTOSE MALABSORPTION CAUSED BY A DEFECT IN THE NA+/GLUCOSE COTRANSPORTER [J].
TURK, E ;
ZABEL, B ;
MUNDLOS, S ;
DYER, J ;
WRIGHT, EM .
NATURE, 1991, 350 (6316) :354-356
[2]  
WRIGHT EM, 2001, METABOLIC MOL BASES, P4891