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Mutation analysis in CNTFRα coding sequence from a patient with glioblastoma. Mutation analysis showing a missense mutation (T151A) in the only patient (W28) of 32 sampled (lower). This mutation occurred in exon 2 and coded for a tryptophan to arginine (W→R) change. Representative sequencing profile for normal CNTFRα exon 2 coding region (upper).
