A Study on Genetic Polymorphism of RET Proto-Oncogene in Hirschsprung's Disease in Children

BACKGROUND: Hirschsprung's disease (HD) is a genetic disorder with a complex pattern of inheritance. Some single-nucleotide polymorphisms (SNPs) are identified to be associated with the risk of Hirschsprung's Disease (HSCR). AIMS AND OBJECTIVES: The aim of this study is to know the associa...

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Detalles Bibliográficos
Autores principales: Kumari, Madhu, Das, Chhanda, Mukhopadhyay, Madhumita, Patra, Rishav Dev, Mitra, Pradip Kumar, Mukhopadhyay, Biswanath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051638/
https://www.ncbi.nlm.nih.gov/pubmed/33342844
http://dx.doi.org/10.4103/ajps.AJPS_69_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051638/
https://www.ncbi.nlm.nih.gov/pubmed/33342844
http://dx.doi.org/10.4103/ajps.AJPS_69_17

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