The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease
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 and meth...
| Principais autores: | , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | English |
| Publicado em: |
BioMed Central Ltd
2022
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| Assuntos: | |
| Acesso em linha: | https://repository.ugm.ac.id/283783/1/238.pdf |
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