Preliminary study shows novel variant detected in the screening of RET gene in Malaysian patients with Hirschsprung’s disease

Preliminary study shows novel variant detected in the screening of RET gene in Malaysian patients with Hirschsprung’s disease

Hirschsprung’s disease (HSCR) is a disorder associated with congenital absence of ganglion cells in the gastrointestinal tract. Molecular analyses have identified variants in various genes including RET, GDNF, EDN3 and EDNRB that are involved in the development, migration and survival of neural cell...

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Bibliographic Details
Main Authors: Nor Azian Abdul Murad, Then, Sue-Mian, Mohd Ridhwan Abd Razak, Conjeevaram Rajendrarao Thambidorai, Sri Noraima Othman, Rosniza Mohamad Hussain, Mohan Nallusamy, Syed Zulkifli Syed Zakaria, Isa Mohammad Rose, Zarina Latiff, Rahman Jamal
Format: Article
Language:English
Published: Pusat Perubatan Universiti Kebangsaan Malaysia 2017
Online Access:http://journalarticle.ukm.my/13243/
http://journalarticle.ukm.my/13243/1/33-85-1-PB.pdf

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