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Novel mutations of RET gene in Korean patients with sporadic Hirschsprung's disease

✍ Scribed by Jeong-Hyun Kim; Kyong-Oh Yoon; Jeong-Kook Kim; Jong-Won Kim; Suk-Koo Lee; Sun-Young Kong; Jeong-Meen Seo


Book ID
116685899
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
294 KB
Volume
41
Category
Article
ISSN
0022-3468

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## Abstract ## BACKGROUND Hirschsprung disease (HSCR) is a congenital disease characterized by the absence of ganglion cells in various length of distal digestive tract. The rearranged during transfection gene (__RET__) is considered the major gene in HSCR. Although an increasing number of HSCR‐as