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t/gene-mpz

MPZ gene

Discuss publications and research concerning the MPZ gene.

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Related literature

Genetic and clinical spectrums in Korean Charcot-Marie-Tooth disease patients with myelin protein zero mutations.
MPZ
Genetic variants, structural, and functional changes of Myelin Protein Zero and Mannose-Binding Lectin 2 protein involved in immune response and its allelic transmission in families of patients with leprosy in Colombia.
MPZ
A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States.
MPZ
Sural nerve biopsy and functional studies support the pathogenic role of a novel MPZ mutation.
MPZ
[Ultrasound diagnosis of Charcot-Marie-Tooth disease].
MPZ
Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing.
MPZ
Compound Charcot-Marie-Tooth disease: a kindred with severe hereditary neuropathy, pupil abnormalities and a novel MPZ mutation.
MPZ
A novel mutation of myelin protein zero associated with late-onset predominantly axonal Charcot-Marie-Tooth disease.
MPZ
Late-onset CMT phenotype caused by a novel mutation in the MPZ gene.
MPZ
Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a myelin protein zero p.Ile112Thr mutation.
MPZ

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