Pages that link to "Q72160523"
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The following pages link to Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD) (Q72160523):
Displayed 5 items.
- The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking (Q24609096) (← links)
- Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time (Q28507527) (← links)
- High-resolution genetic mapping of the gunmetal gene which regulates platelet production (Q48065788) (← links)
- The gene encoding the thrombin receptor (Cf2r) maps to mouse chromosome 13 (Q71140944) (← links)
- rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping (Q74063817) (← links)