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3.12.2175
3.12.2175
http://dx.doi.org/10.1093/HMG/3.12.2175
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
P356
Q28235848-FB467410-8953-4C76-B657-71E46E2E98E8
P356
3.12.2175
http://dx.doi.org/10.1093/HMG/3.12.2175