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...
| Main Authors: | , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Pusat Perubatan Universiti Kebangsaan Malaysia
2017
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| Online Access: | http://journalarticle.ukm.my/13243/ http://journalarticle.ukm.my/13243/ http://journalarticle.ukm.my/13243/1/33-85-1-PB.pdf |