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RAPID DETECTION OF DUPLICATION/DELETION OF THE PMP22 GENE IN PATIENTS WITH CHARCOT-MARIE-TOUTH DISEASE TYPE 1A AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY BY REAL-TIME QUANTITATIVE PCR USING SYBR GREEN I DYE
KIM S.W. | LEE K.S. | JIN H.S. | LEE T.M. | KOO S.K. | LEE Y.J. | JUNG S.C.
MEDICAL SCIENCE (PARIS)
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