Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease (Q40393824)

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Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease
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    Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease (English)
    Thomas Y Y Leon
    Maria-Mercedes Garcia-Barceló
    Raymond W Ganster
    Benedict L S Chen

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