Binding of PMP2 to the inner leaflet of the basal PM in a PI(4,5)P 2... | Download Scientific Diagram
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A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy | PLOS Genetics
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PMP2/FABP8 induces PI(4,5)P2-dependent transbilayer reorganization of sphingomyelin in the plasma membrane - ScienceDirect
Phenotype of PMP2 transgenic mice. (A) Tail suspension test showed hind... | Download Scientific Diagram
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An autosomal dominant CMT 1 family with PMP2 mutation. (A) Pedigree of... | Download Scientific Diagram
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Children | Free Full-Text | A Novel Family with Demyelinating Charcot–Marie–Tooth Disease Caused by a Mutation in the PMP2 Gene: A Case Series of Nine Patients and a Brief Review of the
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PMP2/FABP8 induces PI(4,5)P2-dependent transbilayer reorganization of sphingomyelin in the plasma membrane - ScienceDirect
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