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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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Detalles Bibliográficos
Publicado en:Ann Transl Med
Autores principales: Musthofa, Fuad Dheni, Rochadi, Gunadi
Formato: Artigo
Lenguaje:Inglês
Publicado: AME Publishing Company 2017
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Acceso en línea: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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