QuickView for PMP2;jsessionid=CA9380380104A13418C0B171D13702F0;jsessionid=E6559D22B92E5FF43CA4079FD68A1A0E;jsessionid=AC261806F0F394E51D46C987F0C37164;jsessionid=74EC6CF0D567462512CD1AE382368FBF (gene)

1. Establishment and characterization of NCC-PMP2-C1: a novel patient-derived cell line of pseudomyxoma…
2. PMP2/FABP8 induces PI(4,5)P2-dependent transbilayer reorganization of sphingomyelin in the plasma me…
3. Early onset demyelinating Charcot-Marie-Tooth disease caused by a novel in-frame isoleucine deletion…
4. Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical…
5. A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.

There were no clinical trials for PMP2;jsessionid=CA9380380104A13418C0B171D13702F0;jsessionid=E6559D22B92E5FF43CA4079FD68A1A0E;jsessionid=AC261806F0F394E51D46C987F0C37164;jsessionid=74EC6CF0D567462512CD1AE382368FBF