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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Format: | Book |
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BMC,
2022-04-01T00:00:00Z.
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A1234.567 |
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