共 50 条
- [42] MOLECULAR-BASIS OF HEREDITARY SPHEROCYTOSIS RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS, 1991, 17 (06): : 696 - 706
- [44] A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2012, 302 (09): : C1405 - C1412
- [48] The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1 BRAIN & DEVELOPMENT, 2015, 37 (01): : 163 - 167
- [50] The Molecular Basis of Glucose Galactose Malabsorption in a Large Swedish Pedigree FUNCTION, 2021, 2 (05):