Hyperekplexia 2
MONDO:0013828Any hereditary hyperekplexia in which the cause of the disease is a mutation in the GLRB gene.
Also known as: GLRB hereditary hyperekplexia, HKPX2, hereditary hyperekplexia caused by mutation in GLRB, hyperekplexia 2, hyperekplexia type 2
12 clinical trials for this condition and its sub-types, 0 tagged with Hyperekplexia 2 itself.
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