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The Journal of Physiology|January 5, 2002
Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1Ruth Rea, Alexander Spauschus, Louise H Eunson, et al.
The European Journal of Neuroscience|August 10, 2002
Functional characterization of compound heterozygosity for GlyRalpha1 mutations in the startle disease hyperekplexiaRuth Rea, Marina A Tijssen, Colin Herd, et al.
Neuron|March 9, 2004
Streamlined synaptic vesicle cycle in cone photoreceptor terminalsRuth Rea, Jian Li, Ajay Dharia, et al.
Neuron|November 23, 2005
Encoding light intensity by the cone photoreceptor synapseSue-Yeon Choi, Bart G Borghuis, Bart Borghuis, et al.
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