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2912923
2912923
https://w3id.org/oc/corpus/br/2912923
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
P3181
0d868c5cf2b71db1c59c07aad5d8e26ca9b62117
P3181
Q28235848-D1E6B69A-0000-4376-913C-37E29FC591D1
P3181
2912923
https://w3id.org/oc/corpus/br/2912923