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4.9.1673
4.9.1673
http://dx.doi.org/10.1093/HMG/4.9.1673
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group
P356
Q70838241-B66E677D-AC3A-48F4-96AE-7090EDF7BB45
P356
4.9.1673
http://dx.doi.org/10.1093/HMG/4.9.1673