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Incidence of RET mutations in patients with Hirschsprung's disease

โœ Scribed by M. Sancandi; I. Ceccherini; M. Costa; M. Fava; B. Chen; Y. Wu; R. Hofstra; T. Laurie; M. Griffths; D. Burge; P.K.H. Tam

Book ID
117152990
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
487 KB
Volume
35
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 HSCRโ€as