The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease

Abstract Background Hirschsprung disease (HSCR) is a complex genetic disorder characterized by the lack of ganglion cells in the intestines. A current study showed that the NRG1 rare variant frequency in Indonesian patients with HSCR is only 0.9%. Here, we investigated the impact of NRG1 expressions...

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Main Authors: Gunadi (Author), Alvin Santoso Kalim (Author), Marcellus (Author), Nova Yuli Prasetyo Budi (Author), Kristy Iskandar (Author)
Format: Book
Published: BMC, 2022-04-01T00:00:00Z.
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