Correlation Engine 2.0
Clear Search sequence regions


Two intercomplementary methods of 17p11.2 duplication/deletion identification have been elaborated: STR allelic variants analysis and direct PMP22 gene dosage measuring by means of quantitative Real- Time PCR. It has been carried out detection and analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine. It has been registered the high level of de novo cases with 17p11.2-duplication. It has been shown the 17p11.2 chromosome region duplication/deletion association with CMT1A and HNPP clinical phenotypes which may be used in differential diagnosis of this type of CMT polyneuropathy.

Citation

N V Hryshchenko, L A Livshits. Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine. T͡Sitologii͡a i genetika. 2009 Jan-Feb;43(1):36-41

Expand section icon Mesh Tags

Expand section icon Substances


PMID: 19663313

View Full Text