Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene - Concepedia

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Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

363

Citations

29

References

1993

Year

Kiyoshi Hayasaka, Masato Himoro, Wataru Sato, Goro Takada, Keiichi Uyemura, Nobuyoshi Shimizu, Thomas D. Bird, P. Michael Conneally, Phillip F. Chance

Nature Genetics

Neurodegenerative DiseasesPeripheral NervesGenetic DisorderMedicineGeneticsDegenerative DiseaseNeurologyNeuroscienceNeuropathologyMyelin P0 GeneNeurogenetics

References

	Year	Citations

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