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Gene therapy for inherited hyperbilirubinemias.
Roy-Chowdhury N, Kadakol A, Sappal BS, Thummala NR, Ghosh SS, Lee SW, Roy-Chowdhury J. Roy-Chowdhury N, et al. Among authors: sappal bs. J Perinatol. 2001 Dec;21 Suppl 1:S114-8; discussion S125-7. doi: 10.1038/sj.jp.7210646. J Perinatol. 2001. PMID: 11803431
Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.
Kadakol A, Sappal BS, Ghosh SS, Lowenheim M, Chowdhury A, Chowdhury S, Santra A, Arias IM, Chowdhury JR, Chowdhury NR. Kadakol A, et al. Among authors: sappal bs. J Med Genet. 2001 Apr;38(4):244-9. doi: 10.1136/jmg.38.4.244. J Med Genet. 2001. PMID: 11370628 Free PMC article. No abstract available.