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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
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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
[DOI] [PMC free article] [PubMed] [Google Scholar] (44).Besemer J
