The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease

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...

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Main Authors: Gunadi, Gunadi, Kalim, Alvin Santoso, Marcellus, Marcellus, Budi, Nova Yuli Prasetyo, Iskandar, Kristy
Format: Article PeerReviewed
Language:English
Published: BioMed Central Ltd 2022
Subjects:
Paediatrics
Online Access:https://repository.ugm.ac.id/283783/1/238.pdf
https://repository.ugm.ac.id/283783/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128459403&doi=10.1186%2fs12887-022-03287-1&partnerID=40&md5=c9813f4b2d7d88bf58109e7316873a80
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Institution: Universitas Gadjah Mada
Language: English

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https://repository.ugm.ac.id/283783/1/238.pdf
https://repository.ugm.ac.id/283783/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85128459403&doi=10.1186%2fs12887-022-03287-1&partnerID=40&md5=c9813f4b2d7d88bf58109e7316873a80

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