Associated Papers
Structure of S1PR2-heterotrimeric G13 signaling complex.
Chen H et al.
Science Advances, 2022
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.
Ingham NJ et al.
Scientific Reports, 2016
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.
Santos-Cortez RL et al.
American Journal of Human Genetics, 2016
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