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Description
L-2-HGA is an autosomal recessive encephalopathy with an onset in childhood that causes developmental delays, epilepsy and cerebellar ataxia, the traditional clinical signs of this condition
Burnell JM, Kirby WM
TRT-HU1 reporter cell-lines stably expressing p Bmal1 -dLuc ( Bmal1 -Luc) were generated using a previously reported transduction protocol for lentivirus-mediated gene delivery 64
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The bank is making progress in controlling costs, though the pace of improvement remains gradual
