Pages that link to "SLC39A4"
From WikiMD's Food, Medicine & Wellness Encyclopedia
← SLC39A4
The following pages link to SLC39A4:
Displayed 32 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Current events (← links | edit)
- List of OMIM disorder codes (← links | edit)
- Gitelman syndrome (← links | edit)
- Hereditary elliptocytosis (← links | edit)
- Pendred syndrome (← links | edit)
- Cystinuria (← links | edit)
- Congenital disorder of glycosylation type IIc (← links | edit)
- Glut1 deficiency (← links | edit)
- Acrodermatitis enteropathica (← links | edit)
- Bantu siderosis (← 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)
- Template:Metal metabolism (← links | edit)
- Vesicular monoamine transporter 1 (← links | edit)
- Wanted articles (← links | edit)
- Adenine nucleotide translocator (← links | edit)
- SCN4B (← links | edit)
- Human iron metabolism (← links | edit)
- MCOLN1 (← links | edit)
- Template:Solute carrier family (← links | edit)
- SAR1B (← links | edit)
- ATP8B3 (← links | edit)
- SLC8B1 (← links | edit)
- SLC13A3 (← links | edit)
- Nav1.4 (← links | edit)
- GLUT5 (← links | edit)
- Sodium/myo-inositol cotransporter (← links | edit)