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- [26] Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: Detection of the recombination 'hotspot' in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 1998, 1 (02) : 495 - 501