Pages that link to "SLC2A10"
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← SLC2A10
The following pages link to SLC2A10:
Displayed 20 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Gitelman syndrome (← links | edit)
- Hereditary elliptocytosis (← links | edit)
- Pendred syndrome (← links | edit)
- Cystinuria (← links | edit)
- Acrodermatitis enteropathica (← links | edit)
- Lysinuric protein intolerance (← links | edit)
- Arterial tortuosity syndrome (← links | edit)
- Allan–Herndon–Dudley syndrome (← links | edit)
- Fanconi–Bickel syndrome (← links | edit)
- Atelosteogenesis type 2 (← links | edit)
- SLC35C1-CDG (CDG-IIc) (← links | edit)
- Glucose transporter type 1 deficiency syndrome (← links | edit)
- Adenine nucleotide translocator (← links | edit)
- SCN4B (← links | edit)
- MCOLN1 (← links | edit)
- Template:Solute carrier family (← links | edit)
- SLC13A3 (← links | edit)
- GLUT5 (← links | edit)
- Sodium/myo-inositol cotransporter (← links | edit)
- Category:Solute carrier family (← links | edit)