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[DOI] [PMC free article] [PubMed] [Google Scholar] 37.Wong A
Moreover, SREBF2 completely lost its potentiation of the ACAT2 promoter transcription when both BS2 and BS3 were deleted
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Hattori, M
Heterozygous parents and siblings of these patients are healthy with no symptoms, which clearly indicates an autosomal recessive disorder
