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AB097. Combined effects of RET transcriptional enhancer variants in Hirschsprung disease

BACKGROUND: Hirschsprung disease (HSCR) is a complex genetic disorder, which characterized by absence of ganglion cells along variable lengths of the intestines in neonates, with the RET was identified as a major locus involved in HSCR. In this study, we investigated the joint effects of common vari...

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Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Musthofa, Fuad Dheni, Rochadi, Gunadi
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641765/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s097
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