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t/gene-pmp22

PMP22 gene

Discuss publications and research concerning the PMP22 gene.

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Related literature

Saposin B Deficiency With Neurologic and Hepatobiliary Involvement: Two Patients Expanding the Clinical Spectrum.
PMP22
Identification and Targeted Correction of a Pathogenic PMP22 Deep Intronic Variant.
PMP22
Prioritization of causal genes from genome-wide association studies by Bayesian data integration across loci.
PMP22
Intermediate conduction velocity in two cases of Charcot-Marie-Tooth disease type 1A.
PMP22
Aberrant miR-29 is a predictive feature of severe phenotypes in pediatric Crohn's disease.
PMP22
Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development.
PMP22
A Computational Approach to Identify a Potential Alternative Drug With Its Positive Impact Toward PMP22.
PMP22
Conformational changes associated with L16P and T118M mutations in the membrane-embedded PMP22 protein, consequential in CMT-1A.
PMP22
Confirmation of the GNB4 gene as causal for Charcot-Marie-Tooth disease by a novel de novo mutation in a Czech patient.
PMP22
[Pathology of Charcot-Marie-Tooth Disease].
PMP22

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